Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130132 |
| ensemblid | ENSG00000162944.11 |
| hgncid | 26402 |
| symbol | RFTN2 |
| name | raftlin family member 2 |
| refseq_nuc | NM_144629.3 |
| refseq_prot | NP_653230.2 |
| ensembl_nuc | ENST00000295049.9 |
| ensembl_prot | ENSP00000295049.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 197568224 |
| end | 197675587 |
| strand | - |
| ver | v1.2 |
| region | chr2:197568224-197675587 |
| region5000 | chr2:197563224-197680587 |
| regionname0 | RFTN2_chr2_197568224_197675587 |
| regionname5000 | RFTN2_chr2_197563224_197680587 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 501 | 307 | 80 | 60 | 136 | 9 | 20 | 112 | RFTN2_chr2_197563224_197680587 | RFTN2 | MGCGL others(496): Show |
chr2 | 197563224 | 197680587 |
| a0002 | 0/0 | 501 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | MGCGL others(496): Show |
chr2 | 197563224 | 197680587 |
| a0003 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | MGCGL others(496): Show |
chr2 | 197563224 | 197680587 |
| a0004 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | MGCGL others(496): Show |
chr2 | 197563224 | 197680587 |
| a0005 | 0/0 | 501 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | MGCGL others(496): Show |
chr2 | 197563224 | 197680587 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1503 | 200 | 69 | 33 | 80 | 6 | 11 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0001c0002 | 1/0 | 1503 | 104 | 10 | 25 | 56 | 3 | 9 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0001c0006 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0001c0007 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0001c0009 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0002c0003 | 0/0 | 1503 | 2 | 0 | 2 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0003c0004 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0004c0008 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 | ||
| a0005c0005 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | ATGGG others(1498): Show |
chr2 | 197563224 | 197680587 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5420 | 66 | 11 | 21 | 22 | 4 | 8 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0002 | 0/0 | 5419 | 3 | 0 | 0 | 3 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0003 | 0/1 | 5420 | 57 | 18 | 10 | 26 | 2 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0004 | 0/0 | 5419 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0005 | 0/0 | 5420 | 17 | 0 | 0 | 17 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0006 | 0/0 | 5421 | 9 | 6 | 0 | 2 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0007 | 0/0 | 5421 | 6 | 2 | 1 | 2 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0008 | 0/0 | 5421 | 5 | 5 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0009 | 0/0 | 5419 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0010 | 0/0 | 5420 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0011 | 0/0 | 5419 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0012 | 0/0 | 5420 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0013 | 0/0 | 5418 | 3 | 3 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5413): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0014 | 0/0 | 5420 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0015 | 0/0 | 5421 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0016 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0017 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0018 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0019 | 0/0 | 5419 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0020 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5411): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0021 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0022 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0023 | 0/0 | 5420 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0024 | 0/0 | 5420 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0025 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0026 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0027 | 0/0 | 5420 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0001t0029 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0001 | 0/0 | 5420 | 5 | 0 | 1 | 4 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0002 | 0/0 | 5419 | 65 | 0 | 22 | 35 | 3 | 5 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0003 | 0/0 | 5420 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0004 | 1/0 | 5419 | 24 | 8 | 0 | 13 | 0 | 2 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0007 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0012 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0028 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0030 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0031 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0032 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0033 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0002t0034 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0001c0006t0006 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| a0001c0007t0001 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0001c0009t0001 | 0/0 | 5420 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0002c0003t0002 | 0/0 | 5419 | 2 | 0 | 2 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0003c0004t0001 | 0/0 | 5420 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5415): Show |
chr2 | 197563224 | 197680587 |
| a0004c0008t0002 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5414): Show |
chr2 | 197563224 | 197680587 |
| a0005c0005t0006 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | GTTAT others(5416): Show |
chr2 | 197563224 | 197680587 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0014g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0015g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0017g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0018g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0019g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0020g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0021g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0022g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0023g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0024g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0025g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0026g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0027g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0029g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0028g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0030g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0031g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0032g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0033g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0034g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0006t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0007t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0009t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0002c0003t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0003c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0004c0008t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0005c0005t0006g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0213 | EUR | FIN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0025 | EUR | FIN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00558 | hp1 | a0001 | c0001 | t0021 | g0129 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00639 | hp1 | a0003 | c0004 | t0001 | g0125 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0272 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0268 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0271 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0255 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0264 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01106 | hp1 | a0001 | c0001 | t0023 | g0162 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0226 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01168 | hp1 | a0001 | c0002 | t0031 | g0230 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01175 | hp2 | a0001 | c0006 | t0006 | g0169 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01255 | hp2 | a0004 | c0008 | t0002 | g0204 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01433 | hp1 | a0001 | c0009 | t0001 | g0308 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01516 | hp1 | a0005 | c0005 | t0006 | g0153 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0244 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0243 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0140 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0242 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0293 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0270 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0266 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02004 | hp1 | a0001 | c0002 | t0030 | g0269 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02015 | hp2 | a0001 | c0001 | t0018 | g0307 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0284 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CDX | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | CDX | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0186 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0189 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0238 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02451 | hp1 | a0001 | c0001 | t0026 | g0206 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0141 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02615 | hp2 | a0001 | c0001 | t0029 | g0052 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0262 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02698 | hp2 | a0001 | c0001 | t0017 | g0299 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0060 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0252 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02809 | hp1 | a0001 | c0001 | t0025 | g0096 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02809 | hp2 | a0001 | c0002 | t0012 | g0008 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0066 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0287 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0288 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02970 | hp1 | a0001 | c0001 | t0022 | g0031 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0055 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03098 | hp2 | a0001 | c0002 | t0028 | g0009 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0054 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0187 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0282 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0078 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03516 | hp2 | a0001 | c0001 | t0020 | g0030 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03654 | hp2 | a0001 | c0002 | t0033 | g0281 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0261 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0289 | SAS | BEB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04199 | hp1 | a0001 | c0002 | t0032 | g0273 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0152 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0210 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0283 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18950 | hp1 | a0001 | c0002 | t0007 | g0231 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18957 | hp2 | a0001 | c0001 | t0014 | g0010 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18961 | hp1 | a0001 | c0002 | t0004 | g0305 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18962 | hp1 | a0001 | c0002 | t0034 | g0200 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0290 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0274 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0224 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18980 | hp1 | a0001 | c0001 | t0014 | g0015 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0294 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19011 | hp2 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0053 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0101 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0223 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19054 | hp2 | a0001 | c0001 | t0015 | g0120 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19066 | hp2 | a0001 | c0001 | t0024 | g0085 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19075 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19077 | hp1 | a0001 | c0001 | t0027 | g0109 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0225 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0260 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0182 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ASW | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ASW | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0185 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0058 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0190 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0280 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0080 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0159 | REF | REF | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0059 | REF | REF | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572047 | A | C | 1 | a0005 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1467T>G | p.Phe489Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1596/5419 | 1467/1506 | 489/501 | chr2 | 197572047 | |||
| chr2:197617850 | T | G | 1 | a0002 | 2 | HG00735.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.1000A>C | p.Ser334Arg | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/9 | 1129/5419 | 1000/1506 | 334/501 | chr2 | 197617850 | |||
| chr2:197633842 | A | C | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.594T>G | p.Asn198Lys | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/9 | 723/5419 | 594/1506 | 198/501 | chr2 | 197633842 | |||
| chr2:197646565 | G | A | 1 | a0004 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.241C>T | p.Pro81Ser | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/9 | 370/5419 | 241/1506 | 81/501 | chr2 | 197646565 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572071 | G | A | 1 | a0001c0006 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1443C>T | p.Leu481Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1572/5419 | 1443/1506 | 481/501 | chr2 | 197572071 | |||
| chr2:197596024 | T | G | 1 | a0001c0007 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1200A>C | p.Pro400Pro | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/9 | 1329/5419 | 1200/1506 | 400/501 | chr2 | 197596024 | |||
| chr2:197644227 | G | A | 6 | a0001c0001 a0001c0006 a0001c0007 others(3): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
synonymous_variant | LOW | c.369C>T | p.Leu123Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/9 | 498/5419 | 369/1506 | 123/501 | chr2 | 197644227 | |||
| chr2:197675450 | G | A | 1 | a0001c0009 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.9C>T | p.Cys3Cys | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/9 | 138/5419 | 9/1506 | 3/501 | chr2 | 197675450 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197568381 | A | G | 4 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0021 others(1): Show |
21 | HG00558.hp1 HG02083.hp2 HG02523.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3627T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3627 | chr2 | 197568381 | ||||||
| chr2:197568456 | A | G | 1 | a0001c0001t0025 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3552T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3552 | chr2 | 197568456 | ||||||
| chr2:197568532 | T | C | 1 | a0001c0001t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3476A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3476 | chr2 | 197568532 | ||||||
| chr2:197568690 | C | T | 1 | a0001c0001t0024 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3318G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3318 | chr2 | 197568690 | ||||||
| chr2:197568961 | TCTC | T | 2 | a0001c0001t0013 a0001c0001t0020 |
4 | HG02818.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3044_*3046delGAG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3044 | chr2 | 197568961 | ||||||
| chr2:197568973 | G | A | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3035C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3035 | chr2 | 197568973 | ||||||
| chr2:197569154 | G | T | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2854C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2854 | chr2 | 197569154 | ||||||
| chr2:197569595 | G | A | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(19): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2413C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2413 | chr2 | 197569595 | ||||||
| chr2:197569676 | C | T | 1 | a0001c0001t0023 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2332 | chr2 | 197569676 | ||||||
| chr2:197569685 | G | A | 1 | a0001c0002t0031 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2323C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2323 | chr2 | 197569685 | ||||||
| chr2:197569788 | C | T | 3 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0028 |
4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2220G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2220 | chr2 | 197569788 | ||||||
| chr2:197569890 | C | T | 1 | a0001c0002t0030 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2118 | chr2 | 197569890 | ||||||
| chr2:197569919 | G | T | 1 | a0001c0001t0022 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2089C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2089 | chr2 | 197569919 | ||||||
| chr2:197569929 | C | CA | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(20): Show |
169 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*2078dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2078 | chr2 | 197569929 | ||||||
| chr2:197569929 | C | CAA | 9 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(6): Show |
30 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2077_*2078dupTT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2078 | chr2 | 197569929 | ||||||
| chr2:197570363 | T | C | 1 | a0001c0001t0027 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1645 | chr2 | 197570363 | ||||||
| chr2:197570386 | C | A | 3 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0016 |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1622G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1622 | chr2 | 197570386 | ||||||
| chr2:197570556 | A | G | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0030 others(5): Show |
75 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1452T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1452 | chr2 | 197570556 | ||||||
| chr2:197570667 | T | C | 1 | a0001c0002t0034 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1341 | chr2 | 197570667 | ||||||
| chr2:197570672 | G | A | 1 | a0001c0002t0028 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1336 | chr2 | 197570672 | ||||||
| chr2:197570725 | G | A | 1 | a0001c0001t0016 | 2 | HG01891.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1283C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1283 | chr2 | 197570725 | ||||||
| chr2:197570748 | C | A | 1 | a0001c0001t0029 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1260 | chr2 | 197570748 | ||||||
| chr2:197571379 | A | G | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(33): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*629T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 629 | chr2 | 197571379 | ||||||
| chr2:197571585 | A | AG | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(16): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*423insC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 422 | chr2 | 197571585 | ||||||
| chr2:197571590 | A | T | 1 | a0001c0001t0017 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 418 | chr2 | 197571590 | ||||||
| chr2:197571616 | G | A | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*392C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 392 | chr2 | 197571616 | ||||||
| chr2:197571667 | C | T | 1 | a0001c0001t0014 | 2 | NA18957.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 341 | chr2 | 197571667 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572423 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1234-143G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572423 | |||||||
| chr2:197572548 | C | T | 4 | a0001c0001t0012g0041 a0001c0001t0012g0149 a0001c0002t0012g0008 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-268G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572548 | |||||||
| chr2:197572553 | C | T | 1 | a0001c0002t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1234-273G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572553 | |||||||
| chr2:197572662 | C | G | 193 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1234-382G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572662 | |||||||
| chr2:197572701 | T | C | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-421A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572701 | |||||||
| chr2:197572743 | T | C | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1234-463A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572743 | |||||||
| chr2:197572805 | TG | T | 17 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0049 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1234-526delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572805 | |||||||
| chr2:197572860 | A | G | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1234-580T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572860 | |||||||
| chr2:197573012 | C | T | 1 | a0001c0001t0007g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1234-732G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573012 | |||||||
| chr2:197573105 | G | A | 49 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(46): Show |
51 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1234-825C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573105 | |||||||
| chr2:197573112 | G | T | 4 | a0001c0001t0012g0041 a0001c0001t0012g0149 a0001c0002t0012g0008 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-832C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573112 | |||||||
| chr2:197573114 | G | A | 2 | a0001c0001t0006g0152 a0005c0005t0006g0153 |
2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-834C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573114 | |||||||
| chr2:197573299 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-1019C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573299 | |||||||
| chr2:197573393 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1234-1113G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573393 | |||||||
| chr2:197573576 | G | A | 2 | a0001c0001t0006g0152 a0005c0005t0006g0153 |
2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-1296C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573576 | |||||||
| chr2:197573583 | T | C | 1 | a0001c0002t0002g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-1303A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573583 | |||||||
| chr2:197573701 | T | C | 97 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1234-1421A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573701 | |||||||
| chr2:197573892 | C | T | 6 | a0001c0002t0002g0211 a0001c0002t0002g0212 a0001c0002t0002g0238 others(3): Show |
6 | HG01256.hp2 HG01258.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1612G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573892 | |||||||
| chr2:197574318 | G | C | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-2038C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574318 | |||||||
| chr2:197574376 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-2096A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574376 | |||||||
| chr2:197574397 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1234-2117T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574397 | |||||||
| chr2:197574536 | AC | A | 119 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-2257delG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574536 | |||||||
| chr2:197574590 | G | T | 1 | a0001c0001t0003g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1234-2310C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574590 | |||||||
| chr2:197574870 | AAAAC | A | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1234-2594_1234-259 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574870 | |||||||
| chr2:197574999 | G | A | 1 | a0001c0001t0009g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1234-2719C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574999 | |||||||
| chr2:197575191 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1234-2911C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575191 | |||||||
| chr2:197575380 | G | A | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3100C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575380 | |||||||
| chr2:197575647 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1234-3367G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575647 | |||||||
| chr2:197575753 | A | T | 2 | a0001c0001t0011g0136 a0001c0001t0011g0184 |
2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1234-3473T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575753 | |||||||
| chr2:197575753 | AT | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG00642.hp1 HG01070.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1234-3474delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575753 | |||||||
| chr2:197575761 | T | A | 2 | a0001c0002t0002g0238 a0001c0002t0002g0257 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1234-3481A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575761 | |||||||
| chr2:197575792 | TTA | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(1): Show |
6 | HG02559.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-3514_1234-351 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575792 | |||||||
| chr2:197575794 | A | ATATATAT others(22): Show |
61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(58): Show |
63 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1234-3543_1234-351 others(33): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575794 | |||||||
| chr2:197575796 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0009g0045 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1234-3516T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575796 | |||||||
| chr2:197575832 | ATATAT | A | 119 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-3557_1234-355 others(9): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575832 | |||||||
| chr2:197575847 | T | A | 3 | a0001c0001t0005g0082 a0002c0003t0002g0226 a0002c0003t0002g0255 |
3 | HG00735.hp1 HG01106.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1234-3567A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575847 | |||||||
| chr2:197575849 | T | G | 4 | a0001c0002t0002g0133 a0001c0002t0002g0210 a0001c0002t0002g0227 others(1): Show |
4 | HG01099.hp1 HG01123.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-3569A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575849 | |||||||
| chr2:197575879 | TTATATAT others(2): Show |
T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG01243.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3608_1234-360 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575879 | |||||||
| chr2:197575896 | A | AAT | 6 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0002t0002g0221 others(3): Show |
6 | HG00621.hp1 HG02027.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-3618_1234-361 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575896 | |||||||
| chr2:197575935 | G | GCTAAGTC others(5): Show |
1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-3656_1234-365 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575935 | |||||||
| chr2:197575936 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-3656C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575936 | |||||||
| chr2:197575993 | G | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1234-3713C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575993 | |||||||
| chr2:197576015 | T | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0021 a0001c0001t0003g0022 |
4 | NA18946.hp1 NA18951.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-3735A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576015 | |||||||
| chr2:197576075 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1234-3795G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576075 | |||||||
| chr2:197576157 | C | T | 4 | a0001c0002t0002g0133 a0001c0002t0002g0210 a0001c0002t0002g0227 others(1): Show |
4 | HG01099.hp1 HG01123.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-3877G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576157 | |||||||
| chr2:197576295 | T | C | 1 | a0001c0002t0004g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1234-4015A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576295 | |||||||
| chr2:197576468 | A | G | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1234-4188T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576468 | |||||||
| chr2:197576776 | T | C | 1 | a0001c0002t0002g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1234-4496A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576776 | |||||||
| chr2:197576887 | C | T | 1 | a0001c0001t0017g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1234-4607G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576887 | |||||||
| chr2:197577298 | G | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1234-5018C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577298 | |||||||
| chr2:197577560 | A | G | 1 | a0001c0002t0002g0254 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1234-5280T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577560 | |||||||
| chr2:197577766 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG00099.hp2 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-5486G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577766 | |||||||
| chr2:197578088 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-5808C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578088 | |||||||
| chr2:197578145 | T | C | 1 | a0001c0001t0003g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1234-5865A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578145 | |||||||
| chr2:197578371 | AAC | A | 120 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1234-6093_1234-609 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578371 | |||||||
| chr2:197578385 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1234-6105A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578385 | |||||||
| chr2:197578762 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-6482G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578762 | |||||||
| chr2:197578809 | C | G | 2 | a0001c0001t0003g0051 a0001c0001t0003g0065 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-6529G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578809 | |||||||
| chr2:197578932 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1234-6652G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578932 | |||||||
| chr2:197578999 | C | T | 4 | a0001c0002t0002g0218 a0001c0002t0002g0264 a0001c0002t0002g0265 others(1): Show |
4 | HG00738.hp2 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-6719G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578999 | |||||||
| chr2:197579055 | T | C | 1 | a0001c0002t0004g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1234-6775A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579055 | |||||||
| chr2:197579098 | G | A | 1 | a0001c0002t0002g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-6818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579098 | |||||||
| chr2:197579419 | C | T | 1 | a0001c0002t0002g0245 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1234-7139G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579419 | |||||||
| chr2:197579473 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-7193A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579473 | |||||||
| chr2:197579614 | G | A | 1 | a0001c0002t0002g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-7334C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579614 | |||||||
| chr2:197579646 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0024g0085 |
2 | HG00673.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1234-7366A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579646 | |||||||
| chr2:197579899 | C | G | 120 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1234-7619G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579899 | |||||||
| chr2:197579961 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-7681C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579961 | |||||||
| chr2:197580094 | C | T | 2 | a0001c0001t0003g0072 a0001c0001t0006g0176 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1234-7814G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580094 | |||||||
| chr2:197580147 | T | C | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1234-7867A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580147 | |||||||
| chr2:197580157 | C | T | 6 | a0001c0001t0003g0062 a0001c0001t0003g0154 a0001c0001t0011g0136 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-7877G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580157 | |||||||
| chr2:197580245 | T | C | 1 | a0001c0002t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1234-7965A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580245 | |||||||
| chr2:197580450 | C | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0065 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-8170G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580450 | |||||||
| chr2:197580450 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-8170G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580450 | |||||||
| chr2:197580607 | C | A | 4 | a0001c0001t0009g0045 a0001c0001t0009g0046 a0001c0001t0009g0047 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-8327G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580607 | |||||||
| chr2:197580821 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-8541C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580821 | |||||||
| chr2:197580877 | T | C | 206 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(203): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1234-8597A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580877 | |||||||
| chr2:197580878 | G | A | 54 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1234-8598C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580878 | |||||||
| chr2:197580984 | C | T | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1234-8704G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580984 | |||||||
| chr2:197581053 | T | C | 304 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.1234-8773A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581053 | |||||||
| chr2:197581234 | T | C | 1 | a0001c0001t0003g0007 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1234-8954A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581234 | |||||||
| chr2:197581584 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1234-9304G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581584 | |||||||
| chr2:197581656 | A | AC | 6 | a0001c0001t0001g0103 a0001c0001t0001g0127 a0001c0001t0003g0191 others(3): Show |
6 | HG00621.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-9377dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581656 | |||||||
| chr2:197582135 | T | C | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1234-9855A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582135 | |||||||
| chr2:197582261 | C | T | 1 | a0001c0002t0012g0008 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1234-9981G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582261 | |||||||
| chr2:197582262 | G | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-9982C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582262 | |||||||
| chr2:197582335 | C | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10055G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582335 | |||||||
| chr2:197582488 | A | C | 1 | a0001c0002t0002g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-10208T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582488 | |||||||
| chr2:197582549 | C | T | 12 | a0001c0002t0002g0194 a0001c0002t0002g0216 a0001c0002t0002g0217 others(9): Show |
12 | HG00673.hp1 HG02056.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-10269G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582549 | |||||||
| chr2:197582653 | T | A | 1 | a0001c0002t0004g0274 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1234-10373A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582653 | |||||||
| chr2:197582684 | T | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-10404A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582684 | |||||||
| chr2:197582814 | G | A | 2 | a0001c0001t0006g0152 a0005c0005t0006g0153 |
2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-10534C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582814 | |||||||
| chr2:197582934 | G | A | 1 | a0001c0002t0002g0289 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1234-10654C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582934 | |||||||
| chr2:197582951 | C | T | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-10671G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582951 | |||||||
| chr2:197583022 | C | A | 1 | a0001c0001t0003g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1234-10742G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583022 | |||||||
| chr2:197583100 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10820G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583100 | |||||||
| chr2:197583101 | G | A | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1234-10821C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583101 | |||||||
| chr2:197583129 | A | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10849T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583129 | |||||||
| chr2:197583272 | T | A | 1 | a0001c0001t0003g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1234-10992A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583272 | |||||||
| chr2:197583614 | G | A | 119 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-11334C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583614 | |||||||
| chr2:197583624 | C | CT | 7 | a0001c0001t0001g0105 a0001c0001t0001g0147 a0001c0001t0001g0207 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234-11345dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583624 | |||||||
| chr2:197583624 | CT | C | 11 | a0001c0001t0001g0050 a0001c0001t0001g0296 a0001c0001t0003g0040 others(8): Show |
11 | HG01517.hp2 HG01884.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-11345delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583624 | |||||||
| chr2:197583643 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-11363A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583643 | |||||||
| chr2:197583691 | C | T | 1 | a0001c0001t0025g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1234-11411G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583691 | |||||||
| chr2:197583703 | T | C | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-11423A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583703 | |||||||
| chr2:197583953 | G | A | 2 | a0001c0001t0012g0041 a0001c0001t0012g0149 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1234-11673C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583953 | |||||||
| chr2:197583973 | C | CT | 206 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(203): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1234-11694_1234-11 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583973 | |||||||
| chr2:197584312 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0019g0187 |
2 | HG00738.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1233+11679G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197584312 | |||||||
| chr2:197584716 | G | A | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1233+11275C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197584716 | |||||||
| chr2:197585014 | G | A | 2 | a0001c0001t0005g0082 a0001c0001t0005g0132 |
2 | HG02523.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1233+10977C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585014 | |||||||
| chr2:197585070 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1233+10921C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585070 | |||||||
| chr2:197585133 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1233+10858C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585133 | |||||||
| chr2:197585306 | A | T | 204 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1233+10685T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585306 | |||||||
| chr2:197585354 | C | A | 1 | a0001c0002t0004g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1233+10637G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585354 | |||||||
| chr2:197585692 | C | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+10299G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585692 | |||||||
| chr2:197585738 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+10253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585738 | |||||||
| chr2:197585739 | G | A | 1 | a0001c0001t0003g0011 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1233+10252C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585739 | |||||||
| chr2:197585761 | C | T | 1 | a0001c0002t0030g0269 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1233+10230G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585761 | |||||||
| chr2:197586135 | G | A | 1 | a0001c0002t0002g0240 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1233+9856C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586135 | |||||||
| chr2:197586158 | C | T | 4 | a0001c0001t0011g0136 a0001c0001t0011g0157 a0001c0001t0011g0184 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+9833G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586158 | |||||||
| chr2:197586191 | G | C | 1 | a0001c0001t0005g0181 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1233+9800C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586191 | |||||||
| chr2:197586229 | C | T | 1 | a0001c0002t0004g0259 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1233+9762G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586229 | |||||||
| chr2:197586271 | T | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9720A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586271 | |||||||
| chr2:197586386 | G | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9605C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586386 | |||||||
| chr2:197586529 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233+9462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586529 | |||||||
| chr2:197586534 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0007g0092 |
3 | HG01069.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1233+9457G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586534 | |||||||
| chr2:197586818 | G | A | 2 | a0001c0002t0002g0256 a0001c0002t0031g0230 |
2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1233+9173C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586818 | |||||||
| chr2:197586867 | T | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9124A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586867 | |||||||
| chr2:197586953 | C | G | 1 | a0001c0002t0002g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1233+9038G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586953 | |||||||
| chr2:197587031 | C | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+8960G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587031 | |||||||
| chr2:197587177 | C | A | 1 | a0001c0002t0002g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1233+8814G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587177 | |||||||
| chr2:197587367 | C | T | 3 | a0001c0001t0003g0163 a0001c0001t0003g0170 a0001c0001t0023g0162 |
3 | HG01070.hp2 HG01106.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1233+8624G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587367 | |||||||
| chr2:197587401 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+8590C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587401 | |||||||
| chr2:197587529 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+8462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587529 | |||||||
| chr2:197587630 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1233+8361G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587630 | |||||||
| chr2:197587693 | G | A | 4 | a0001c0001t0011g0136 a0001c0001t0011g0157 a0001c0001t0011g0184 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+8298C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587693 | |||||||
| chr2:197587801 | A | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+8190T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587801 | |||||||
| chr2:197587874 | G | A | 1 | a0001c0001t0005g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+8117C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587874 | |||||||
| chr2:197587934 | A | G | 1 | a0001c0002t0002g0277 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1233+8057T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587934 | |||||||
| chr2:197588113 | T | C | 1 | a0001c0001t0005g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1233+7878A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588113 | |||||||
| chr2:197588258 | G | C | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+7733C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588258 | |||||||
| chr2:197588355 | T | A | 1 | a0001c0001t0010g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1233+7636A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588355 | |||||||
| chr2:197588394 | T | C | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+7597A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588394 | |||||||
| chr2:197588721 | T | C | 1 | a0001c0002t0002g0257 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1233+7270A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588721 | |||||||
| chr2:197588796 | C | G | 1 | a0001c0001t0005g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+7195G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588796 | |||||||
| chr2:197588885 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1233+7106G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588885 | |||||||
| chr2:197588961 | C | T | 114 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1233+7030G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588961 | |||||||
| chr2:197589006 | G | A | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+6985C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589006 | |||||||
| chr2:197589012 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+6979T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589012 | |||||||
| chr2:197589145 | T | C | 1 | a0001c0001t0007g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1233+6846A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589145 | |||||||
| chr2:197589217 | C | A | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+6774G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589217 | |||||||
| chr2:197589219 | C | CA | 29 | a0001c0001t0002g0156 a0001c0001t0006g0148 a0001c0001t0007g0076 others(26): Show |
29 | HG00673.hp1 HG01099.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1233+6771dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | C | CAA | 44 | a0001c0001t0002g0155 a0001c0001t0006g0150 a0001c0001t0008g0185 others(41): Show |
44 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1233+6770_1233+677 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | C | CAAA | 19 | a0001c0001t0006g0151 a0001c0002t0002g0183 a0001c0002t0002g0202 others(16): Show |
19 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1233+6769_1233+677 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | C | CAAAA | 9 | a0001c0001t0018g0307 a0001c0002t0002g0238 a0001c0002t0002g0241 others(6): Show |
9 | HG00733.hp2 HG01928.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+6768_1233+677 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CA | C | 34 | a0001c0001t0001g0172 a0001c0001t0001g0177 a0001c0001t0001g0300 others(31): Show |
34 | HG01175.hp2 HG01243.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.1233+6771delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CAA | C | 64 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0069 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1233+6770_1233+677 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CAAA | C | 69 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1233+6769_1233+677 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CAAAA | C | 7 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0201 others(4): Show |
7 | HG01070.hp1 HG01891.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+6768_1233+677 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1233+6760_1233+677 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589219 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0003g0062 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+6756_1233+677 others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | |||||||
| chr2:197589355 | G | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+6636C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589355 | |||||||
| chr2:197589555 | T | C | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+6436A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589555 | |||||||
| chr2:197589616 | T | C | 2 | a0001c0001t0007g0078 a0001c0001t0025g0096 |
2 | HG02809.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1233+6375A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589616 | |||||||
| chr2:197589807 | T | C | 1 | a0001c0001t0010g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1233+6184A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589807 | |||||||
| chr2:197589967 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1233+6024G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589967 | |||||||
| chr2:197590056 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590056 | |||||||
| chr2:197590066 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
48 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1233+5925G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590066 | |||||||
| chr2:197590126 | C | A | 6 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(3): Show |
6 | HG02015.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+5865G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590126 | |||||||
| chr2:197590194 | C | T | 1 | a0001c0001t0006g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1233+5797G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590194 | |||||||
| chr2:197590195 | G | A | 1 | a0001c0002t0002g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1233+5796C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590195 | |||||||
| chr2:197590239 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1233+5752C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590239 | |||||||
| chr2:197590319 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5672A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590319 | |||||||
| chr2:197590449 | C | T | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1233+5542G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590449 | |||||||
| chr2:197590575 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1233+5416A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590575 | |||||||
| chr2:197590617 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1233+5374A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590617 | |||||||
| chr2:197590620 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1233+5371A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590620 | |||||||
| chr2:197590634 | G | A | 2 | a0001c0002t0012g0008 a0001c0002t0028g0009 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1233+5357C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590634 | |||||||
| chr2:197590705 | C | G | 119 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1233+5286G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590705 | |||||||
| chr2:197590725 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1233+5266G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590725 | |||||||
| chr2:197590743 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1233+5248C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590743 | |||||||
| chr2:197590793 | G | T | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+5198C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590793 | |||||||
| chr2:197590798 | C | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+5193G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590798 | |||||||
| chr2:197590808 | C | T | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+5183G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590808 | |||||||
| chr2:197590829 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5162G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590829 | |||||||
| chr2:197590883 | G | A | 44 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(41): Show |
46 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1233+5108C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590883 | |||||||
| chr2:197590893 | A | T | 1 | a0001c0001t0005g0116 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1233+5098T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590893 | |||||||
| chr2:197590921 | A | T | 2 | a0001c0002t0002g0211 a0001c0002t0002g0212 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1233+5070T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590921 | |||||||
| chr2:197590970 | G | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5021C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590970 | |||||||
| chr2:197590997 | TG | T | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4993delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590997 | |||||||
| chr2:197591202 | C | T | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1233+4789G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591202 | |||||||
| chr2:197591268 | A | T | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4723T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591268 | |||||||
| chr2:197591340 | T | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
48 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1233+4651A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591340 | |||||||
| chr2:197591410 | C | T | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+4581G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591410 | |||||||
| chr2:197591495 | A | G | 2 | a0002c0003t0002g0226 a0002c0003t0002g0255 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1233+4496T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591495 | |||||||
| chr2:197591528 | G | A | 1 | a0001c0001t0005g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+4463C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591528 | |||||||
| chr2:197591573 | C | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+4418G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591573 | |||||||
| chr2:197591578 | C | A | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+4413G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591578 | |||||||
| chr2:197591586 | C | A | 98 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1233+4405G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591586 | |||||||
| chr2:197591616 | T | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG01099.hp2 HG01243.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+4375A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591616 | |||||||
| chr2:197591658 | G | C | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+4333C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591658 | |||||||
| chr2:197591702 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1233+4289C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591702 | |||||||
| chr2:197591735 | G | A | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1233+4256C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591735 | |||||||
| chr2:197591776 | G | A | 2 | a0001c0002t0012g0008 a0001c0002t0028g0009 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1233+4215C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591776 | |||||||
| chr2:197591812 | G | C | 3 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 |
3 | HG00408.hp1 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1233+4179C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591812 | |||||||
| chr2:197591825 | C | T | 1 | a0001c0001t0003g0016 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1233+4166G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591825 | |||||||
| chr2:197591909 | C | T | 5 | a0001c0001t0003g0062 a0001c0001t0009g0045 a0001c0001t0009g0046 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4082G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591909 | |||||||
| chr2:197591932 | G | GCCTCTCC others(7): Show |
2 | a0002c0003t0002g0226 a0002c0003t0002g0255 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1233+4045_1233+405 others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591932 | |||||||
| chr2:197592073 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1233+3918C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592073 | |||||||
| chr2:197592159 | G | C | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1233+3832C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592159 | |||||||
| chr2:197592203 | T | A | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3788A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592203 | |||||||
| chr2:197592385 | G | A | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3606C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592385 | |||||||
| chr2:197592495 | G | C | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3496C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592495 | |||||||
| chr2:197592569 | T | G | 4 | a0001c0001t0013g0048 a0001c0001t0013g0066 a0001c0001t0013g0101 others(1): Show |
4 | HG02818.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+3422A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592569 | |||||||
| chr2:197593122 | T | C | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+2869A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593122 | |||||||
| chr2:197593555 | A | AT | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
48 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1233+2435dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593555 | |||||||
| chr2:197593655 | G | A | 1 | a0001c0002t0002g0270 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1233+2336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593655 | |||||||
| chr2:197593716 | A | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+2275T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593716 | |||||||
| chr2:197593720 | C | G | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+2271G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593720 | |||||||
| chr2:197593807 | A | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+2184T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593807 | |||||||
| chr2:197594015 | C | CT | 11 | a0001c0002t0002g0216 a0001c0002t0002g0243 a0001c0002t0002g0251 others(8): Show |
11 | HG01106.hp2 HG01517.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+1975dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594015 | |||||||
| chr2:197594015 | CT | C | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1233+1975delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594015 | |||||||
| chr2:197594078 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+1913G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594078 | |||||||
| chr2:197594173 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1233+1818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594173 | |||||||
| chr2:197594241 | C | T | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+1750G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594241 | |||||||
| chr2:197594429 | G | C | 4 | a0001c0001t0011g0136 a0001c0001t0011g0157 a0001c0001t0011g0184 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1562C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594429 | |||||||
| chr2:197594622 | G | A | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+1369C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594622 | |||||||
| chr2:197594659 | T | C | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+1332A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594659 | |||||||
| chr2:197594692 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1233+1299A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594692 | |||||||
| chr2:197594821 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+1170G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594821 | |||||||
| chr2:197594999 | G | T | 1 | a0001c0002t0002g0289 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1233+992C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594999 | |||||||
| chr2:197595008 | T | C | 2 | a0001c0002t0002g0193 a0001c0002t0034g0200 |
2 | NA18962.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1233+983A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595008 | |||||||
| chr2:197595114 | A | C | 1 | a0001c0002t0004g0282 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1233+877T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595114 | |||||||
| chr2:197595316 | T | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
48 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1233+675A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595316 | |||||||
| chr2:197595353 | C | A | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+638G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595353 | |||||||
| chr2:197595618 | A | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+373T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595618 | |||||||
| chr2:197596215 | T | C | 2 | a0001c0001t0003g0165 a0001c0001t0006g0164 |
2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1155-146A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596215 | |||||||
| chr2:197596355 | C | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0177 a0001c0001t0007g0067 |
3 | HG00621.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1155-286G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596355 | |||||||
| chr2:197596429 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1155-360G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596429 | |||||||
| chr2:197596887 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1155-818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596887 | |||||||
| chr2:197597174 | T | C | 1 | a0001c0002t0002g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1155-1105A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197597174 | |||||||
| chr2:197597217 | A | C | 73 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(70): Show |
75 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1155-1148T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197597217 | |||||||
| chr2:197598133 | A | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0172 a0001c0001t0001g0296 others(2): Show |
5 | HG01884.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-2064T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598133 | |||||||
| chr2:197598218 | G | C | 8 | a0001c0001t0001g0137 a0001c0001t0003g0062 a0001c0001t0009g0045 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-2149C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598218 | |||||||
| chr2:197598366 | G | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1155-2297C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598366 | |||||||
| chr2:197598586 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-2517A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598586 | |||||||
| chr2:197598781 | G | T | 1 | a0001c0002t0002g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1155-2712C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598781 | |||||||
| chr2:197598958 | CT | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0303 others(3): Show |
6 | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155-2890delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598958 | |||||||
| chr2:197598967 | T | G | 29 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(26): Show |
29 | HG00621.hp2 HG00735.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1155-2898A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598967 | |||||||
| chr2:197598998 | C | A | 1 | a0001c0001t0003g0011 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1155-2929G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598998 | |||||||
| chr2:197599033 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-2964C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599033 | |||||||
| chr2:197599484 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1155-3415G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599484 | |||||||
| chr2:197599595 | T | C | 1 | a0001c0002t0033g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1155-3526A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599595 | |||||||
| chr2:197599733 | G | C | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-3664C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599733 | |||||||
| chr2:197599866 | TA | T | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-3798delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599866 | |||||||
| chr2:197599885 | T | A | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-3816A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599885 | |||||||
| chr2:197600029 | T | C | 1 | a0001c0001t0008g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1155-3960A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600029 | |||||||
| chr2:197600209 | C | T | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155-4140G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600209 | |||||||
| chr2:197600552 | C | T | 2 | a0001c0001t0003g0165 a0001c0001t0006g0164 |
2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1155-4483G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600552 | |||||||
| chr2:197600719 | C | T | 1 | a0001c0001t0009g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1155-4650G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600719 | |||||||
| chr2:197600833 | T | C | 1 | a0001c0002t0002g0220 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1155-4764A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600833 | |||||||
| chr2:197600837 | C | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-4768G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600837 | |||||||
| chr2:197600973 | G | A | 9 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0002t0002g0221 others(6): Show |
9 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155-4904C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600973 | |||||||
| chr2:197601043 | G | C | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-4974C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601043 | |||||||
| chr2:197601116 | T | C | 119 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1155-5047A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601116 | |||||||
| chr2:197601190 | T | C | 4 | a0001c0002t0002g0183 a0001c0002t0002g0268 a0001c0002t0002g0271 others(1): Show |
4 | HG00642.hp2 HG00733.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-5121A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601190 | |||||||
| chr2:197601307 | A | G | 1 | a0001c0001t0010g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1155-5238T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601307 | |||||||
| chr2:197601313 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-5244A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601313 | |||||||
| chr2:197601400 | T | C | 11 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155-5331A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601400 | |||||||
| chr2:197601549 | T | C | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1155-5480A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601549 | |||||||
| chr2:197601567 | A | C | 2 | a0001c0001t0006g0148 a0001c0001t0006g0150 |
2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-5498T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601567 | |||||||
| chr2:197601586 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1155-5517G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601586 | |||||||
| chr2:197601674 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1155-5605A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601674 | |||||||
| chr2:197601738 | C | A | 74 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(71): Show |
76 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1155-5669G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601738 | |||||||
| chr2:197601781 | A | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0161 a0001c0001t0001g0180 |
3 | HG01168.hp2 HG01255.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1155-5712T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601781 | |||||||
| chr2:197601815 | T | C | 13 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(10): Show |
13 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1155-5746A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601815 | |||||||
| chr2:197602040 | T | C | 1 | a0001c0001t0026g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1155-5971A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602040 | |||||||
| chr2:197602064 | T | A | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155-5995A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602064 | |||||||
| chr2:197602150 | C | T | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1155-6081G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602150 | |||||||
| chr2:197602241 | T | G | 13 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(10): Show |
13 | HG02015.hp2 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1155-6172A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602241 | |||||||
| chr2:197602389 | A | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(41): Show |
46 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1155-6320T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602389 | |||||||
| chr2:197602417 | C | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1155-6348G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602417 | |||||||
| chr2:197602428 | T | A | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-6359A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602428 | |||||||
| chr2:197602634 | G | A | 1 | a0001c0002t0004g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155-6565C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602634 | |||||||
| chr2:197602952 | T | C | 1 | a0001c0002t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1155-6883A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602952 | |||||||
| chr2:197603003 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | NA18946.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1155-6934G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603003 | |||||||
| chr2:197603056 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-6987G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603056 | |||||||
| chr2:197603087 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-7018A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603087 | |||||||
| chr2:197603109 | ATATACCT others(5): Show |
A | 1 | a0001c0001t0003g0011 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1155-7052_1155-704 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603109 | |||||||
| chr2:197603175 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1155-7106G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603175 | |||||||
| chr2:197603182 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1155-7113G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603182 | |||||||
| chr2:197603255 | C | T | 1 | a0001c0001t0016g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1155-7186G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603255 | |||||||
| chr2:197603344 | C | A | 1 | a0001c0001t0006g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1155-7275G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603344 | |||||||
| chr2:197603360 | G | A | 1 | a0001c0001t0006g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1155-7291C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603360 | |||||||
| chr2:197603835 | A | T | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-7766T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603835 | |||||||
| chr2:197604027 | G | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-7958C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604027 | |||||||
| chr2:197604740 | C | CTATT | 6 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0002t0002g0215 others(3): Show |
6 | HG02040.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155-8675_1155-867 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | |||||||
| chr2:197604740 | C | CTATTTAT others(5): Show |
1 | a0001c0002t0002g0289 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1155-8683_1155-867 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | |||||||
| chr2:197604740 | CTATTTAT others(1): Show |
C | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155-8679_1155-867 others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | |||||||
| chr2:197604740 | CTATTTAT others(5): Show |
C | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1155-8683_1155-867 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | |||||||
| chr2:197604740 | CTATTTAT others(9): Show |
C | 1 | a0001c0001t0017g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1155-8687_1155-867 others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | |||||||
| chr2:197604770 | ATTTATTT others(1): Show |
A | 4 | a0001c0002t0002g0218 a0001c0002t0002g0264 a0001c0002t0002g0265 others(1): Show |
4 | HG00738.hp2 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-8709_1155-870 others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604770 | |||||||
| chr2:197604778 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1155-8709A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604778 | |||||||
| chr2:197604795 | C | G | 2 | a0001c0002t0002g0275 a0001c0002t0002g0276 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1155-8726G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604795 | |||||||
| chr2:197604889 | T | C | 1 | a0001c0001t0016g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1155-8820A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604889 | |||||||
| chr2:197604922 | G | A | 7 | a0001c0001t0001g0192 a0001c0001t0003g0007 a0001c0001t0003g0165 others(4): Show |
7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155-8853C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604922 | |||||||
| chr2:197605142 | T | C | 1 | a0001c0001t0005g0035 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1155-9073A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605142 | |||||||
| chr2:197605268 | A | G | 2 | a0001c0001t0006g0148 a0001c0001t0006g0150 |
2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-9199T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605268 | |||||||
| chr2:197605326 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1155-9257A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605326 | |||||||
| chr2:197605407 | G | A | 1 | a0001c0001t0009g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1155-9338C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605407 | |||||||
| chr2:197605409 | G | A | 1 | a0001c0001t0007g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1155-9340C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605409 | |||||||
| chr2:197605426 | A | G | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1155-9357T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605426 | |||||||
| chr2:197605427 | G | C | 1 | a0001c0001t0009g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1155-9358C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605427 | |||||||
| chr2:197605431 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1155-9362C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605431 | |||||||
| chr2:197605432 | A | G | 2 | a0002c0003t0002g0226 a0002c0003t0002g0255 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1155-9363T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605432 | |||||||
| chr2:197605451 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1155-9382T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605451 | |||||||
| chr2:197605458 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1155-9389C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605458 | |||||||
| chr2:197605466 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1155-9397A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605466 | |||||||
| chr2:197605822 | C | T | 45 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(42): Show |
47 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1155-9753G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605822 | |||||||
| chr2:197606172 | T | C | 9 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(6): Show |
9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1154+9704A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606172 | |||||||
| chr2:197606255 | A | C | 1 | a0001c0002t0002g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1154+9621T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606255 | |||||||
| chr2:197606283 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+9593A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606283 | |||||||
| chr2:197606378 | C | T | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+9498G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606378 | |||||||
| chr2:197606666 | G | A | 204 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1154+9210C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606666 | |||||||
| chr2:197606685 | T | G | 1 | a0001c0001t0016g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1154+9191A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606685 | |||||||
| chr2:197606689 | C | T | 1 | a0001c0001t0014g0010 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1154+9187G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606689 | |||||||
| chr2:197607030 | C | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+8846G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607030 | |||||||
| chr2:197607214 | G | A | 1 | a0001c0002t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1154+8662C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607214 | |||||||
| chr2:197607251 | G | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+8625C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607251 | |||||||
| chr2:197607280 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+8596G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607280 | |||||||
| chr2:197607288 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1154+8588G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607288 | |||||||
| chr2:197607354 | T | G | 71 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
73 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.1154+8522A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607354 | |||||||
| chr2:197607457 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0003g0062 a0001c0001t0009g0045 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+8419C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607457 | |||||||
| chr2:197607475 | T | TATA | 18 | a0001c0001t0001g0134 a0001c0001t0001g0172 a0001c0001t0001g0296 others(15): Show |
18 | HG01175.hp2 HG01361.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1154+8398_1154+840 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | T | TATAATA | 49 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(46): Show |
51 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1154+8395_1154+840 others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | T | TATAATAA others(2): Show |
9 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0142 others(6): Show |
11 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1154+8392_1154+840 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | T | TATAATAA others(5): Show |
2 | a0001c0001t0003g0094 a0001c0001t0008g0057 |
2 | HG00733.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1154+8389_1154+840 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | TATA | T | 99 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1154+8398_1154+840 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | TATAATA | T | 3 | a0001c0001t0011g0188 a0001c0001t0018g0307 a0001c0002t0002g0289 |
3 | HG02015.hp2 HG02818.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1154+8395_1154+840 others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607475 | TATAATAA others(2): Show |
T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0007g0092 |
3 | HG01069.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1154+8392_1154+840 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | |||||||
| chr2:197607610 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+8266G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607610 | |||||||
| chr2:197607736 | T | C | 3 | a0001c0002t0002g0005 a0001c0002t0002g0198 a0001c0002t0002g0222 |
3 | HG00558.hp2 HG02165.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1154+8140A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607736 | |||||||
| chr2:197607943 | T | C | 1 | a0001c0002t0002g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1154+7933A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607943 | |||||||
| chr2:197608162 | A | G | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1154+7714T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608162 | |||||||
| chr2:197608310 | A | AT | 60 | a0001c0001t0001g0043 a0001c0001t0001g0115 a0001c0001t0001g0192 others(57): Show |
64 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1154+7565dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608310 | |||||||
| chr2:197608310 | AT | A | 19 | a0001c0001t0001g0113 a0001c0001t0001g0205 a0001c0001t0001g0207 others(16): Show |
19 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1154+7565delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608310 | |||||||
| chr2:197608468 | C | T | 3 | a0001c0001t0011g0136 a0001c0001t0011g0184 a0001c0001t0011g0188 |
3 | HG02486.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1154+7408G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608468 | |||||||
| chr2:197608623 | CT | C | 39 | a0001c0001t0001g0090 a0001c0001t0001g0205 a0001c0001t0001g0207 others(36): Show |
39 | HG01175.hp2 HG01433.hp1 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.1154+7252delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | |||||||
| chr2:197608623 | CTT | C | 149 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(146): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1154+7251_1154+725 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | |||||||
| chr2:197608623 | CTTT | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0091 a0001c0001t0001g0113 others(8): Show |
11 | HG01515.hp1 HG01516.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+7250_1154+725 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | |||||||
| chr2:197608787 | C | T | 1 | a0001c0002t0004g0232 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1154+7089G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608787 | |||||||
| chr2:197608818 | T | C | 2 | a0001c0001t0010g0054 a0001c0001t0010g0055 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1154+7058A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608818 | |||||||
| chr2:197608859 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+7017T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608859 | |||||||
| chr2:197608878 | C | T | 1 | a0001c0002t0002g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1154+6998G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608878 | |||||||
| chr2:197608879 | G | A | 3 | a0001c0001t0011g0136 a0001c0001t0011g0184 a0001c0001t0011g0188 |
3 | HG02486.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1154+6997C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608879 | |||||||
| chr2:197609365 | G | T | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+6511C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609365 | |||||||
| chr2:197609377 | T | C | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+6499A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609377 | |||||||
| chr2:197609403 | A | G | 1 | a0001c0001t0025g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1154+6473T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609403 | |||||||
| chr2:197609494 | A | G | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1154+6382T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609494 | |||||||
| chr2:197609511 | C | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+6365G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609511 | |||||||
| chr2:197609646 | G | A | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1154+6230C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609646 | |||||||
| chr2:197609762 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1154+6114T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609762 | |||||||
| chr2:197609938 | G | A | 2 | a0001c0002t0002g0249 a0001c0002t0002g0292 |
2 | NA18979.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1154+5938C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609938 | |||||||
| chr2:197610184 | C | T | 204 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1154+5692G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610184 | |||||||
| chr2:197610314 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0017g0299 |
2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1154+5562G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610314 | |||||||
| chr2:197610443 | T | G | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1154+5433A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610443 | |||||||
| chr2:197610452 | A | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+5424T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610452 | |||||||
| chr2:197610788 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1154+5088A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610788 | |||||||
| chr2:197610964 | G | A | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+4912C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610964 | |||||||
| chr2:197611055 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+4821C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611055 | |||||||
| chr2:197611056 | A | T | 1 | a0001c0002t0032g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1154+4820T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611056 | |||||||
| chr2:197611129 | A | G | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1154+4747T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611129 | |||||||
| chr2:197611139 | G | T | 2 | a0001c0002t0004g0058 a0001c0002t0004g0060 |
2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1154+4737C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611139 | |||||||
| chr2:197611206 | C | G | 2 | a0001c0001t0012g0041 a0001c0001t0012g0149 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1154+4670G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611206 | |||||||
| chr2:197611262 | C | T | 1 | a0001c0001t0010g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1154+4614G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611262 | |||||||
| chr2:197611414 | T | A | 1 | a0001c0001t0003g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1154+4462A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611414 | |||||||
| chr2:197611419 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1154+4457A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611419 | |||||||
| chr2:197611423 | A | T | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1154+4453T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611423 | |||||||
| chr2:197611428 | A | G | 18 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(15): Show |
18 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1154+4448T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611428 | |||||||
| chr2:197611480 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1154+4396G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611480 | |||||||
| chr2:197611481 | G | A | 1 | a0001c0002t0004g0282 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1154+4395C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611481 | |||||||
| chr2:197611941 | C | T | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+3935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611941 | |||||||
| chr2:197612488 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+3388A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612488 | |||||||
| chr2:197612520 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0091 others(2): Show |
5 | HG00673.hp2 HG03942.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+3356G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612520 | |||||||
| chr2:197612638 | T | C | 1 | a0001c0001t0026g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1154+3238A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612638 | |||||||
| chr2:197612661 | G | A | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1154+3215C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612661 | |||||||
| chr2:197612778 | C | T | 1 | a0001c0002t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1154+3098G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612778 | |||||||
| chr2:197612779 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+3097C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612779 | |||||||
| chr2:197612882 | G | A | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1154+2994C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612882 | |||||||
| chr2:197612896 | C | A | 116 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1154+2980G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612896 | |||||||
| chr2:197613118 | A | G | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154+2758T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613118 | |||||||
| chr2:197613596 | G | A | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1154+2280C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613596 | |||||||
| chr2:197613869 | G | T | 2 | a0001c0001t0009g0045 a0001c0001t0009g0047 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+2007C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613869 | |||||||
| chr2:197613873 | T | C | 2 | a0001c0001t0009g0045 a0001c0001t0009g0047 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+2003A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613873 | |||||||
| chr2:197613912 | G | T | 2 | a0001c0001t0009g0045 a0001c0001t0009g0047 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+1964C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613912 | |||||||
| chr2:197614029 | T | C | 1 | a0001c0002t0002g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1154+1847A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614029 | |||||||
| chr2:197614049 | T | C | 1 | a0001c0002t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1154+1827A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614049 | |||||||
| chr2:197614287 | C | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1154+1589G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614287 | |||||||
| chr2:197614496 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1154+1380C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614496 | |||||||
| chr2:197614614 | C | T | 2 | a0001c0001t0014g0010 a0001c0001t0014g0015 |
2 | NA18957.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1154+1262G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614614 | |||||||
| chr2:197614629 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+1247C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614629 | |||||||
| chr2:197614855 | G | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154+1021C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614855 | |||||||
| chr2:197614950 | C | T | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154+926G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614950 | |||||||
| chr2:197615331 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1154+545T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615331 | |||||||
| chr2:197615348 | G | A | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1154+528C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615348 | |||||||
| chr2:197615371 | T | C | 1 | a0001c0001t0008g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1154+505A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615371 | |||||||
| chr2:197615584 | GT | G | 71 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
73 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.1154+291delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615584 | |||||||
| chr2:197615654 | G | A | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1154+222C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615654 | |||||||
| chr2:197615679 | T | G | 2 | a0001c0001t0009g0045 a0001c0001t0009g0047 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+197A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615679 | |||||||
| chr2:197615849 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1154+27A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615849 | |||||||
| chr2:197615986 | G | C | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1051-7C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197615986 | |||||||
| chr2:197616055 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1051-76G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616055 | |||||||
| chr2:197616131 | A | G | 8 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(5): Show |
8 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051-152T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616131 | |||||||
| chr2:197616135 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1051-156A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616135 | |||||||
| chr2:197616243 | A | G | 1 | a0001c0002t0002g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1051-264T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616243 | |||||||
| chr2:197616268 | C | CATTTT | 94 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0003g0003 others(91): Show |
96 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1051-294_1051-290d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(21): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0079 a0001c0001t0001g0091 others(14): Show |
17 | HG01243.hp2 HG01516.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(30): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(26): Show |
65 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0036 others(62): Show |
65 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(35): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(31): Show |
34 | a0001c0001t0001g0077 a0001c0001t0001g0108 a0001c0001t0001g0114 others(31): Show |
34 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(40): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(36): Show |
5 | a0001c0001t0003g0038 a0001c0001t0005g0124 a0001c0001t0008g0057 others(2): Show |
5 | HG02083.hp2 HG02723.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(45): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(3): Show |
1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1051-299_1051-290d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616268 | C | CATTTTAT others(327): Show |
1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1051-290_1051-289i others(336): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | |||||||
| chr2:197616269 | A | ATTTTATT others(11): Show |
5 | a0001c0001t0003g0062 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG00639.hp1 HG01884.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-291_1051-290i others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616269 | |||||||
| chr2:197616274 | A | ATTTATTT others(5): Show |
4 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-296_1051-295i others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | |||||||
| chr2:197616274 | A | ATTTATTT others(6): Show |
9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0137 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-296_1051-295i others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | |||||||
| chr2:197616274 | A | ATTTATTT others(5): Show |
1 | a0001c0001t0013g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1051-296_1051-295i others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | |||||||
| chr2:197616275 | T | TTTATTTT others(1): Show |
57 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0207 others(54): Show |
59 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.1051-297_1051-296i others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616275 | |||||||
| chr2:197616305 | T | TTTATTTT others(1): Show |
120 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1051-327_1051-326i others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616305 | |||||||
| chr2:197616309 | A | ATTTATTT others(6): Show |
14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0137 others(11): Show |
14 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616309 | A | ATTTTATT others(16): Show |
11 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(8): Show |
13 | HG02132.hp2 HG02300.hp2 HG03209.hp2 others(10): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(25): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616309 | A | ATTTTATT others(21): Show |
45 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(42): Show |
45 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(30): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616309 | A | ATTTTATT others(26): Show |
5 | a0001c0001t0001g0192 a0001c0001t0003g0163 a0001c0001t0003g0170 others(2): Show |
5 | HG01070.hp2 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(35): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616309 | A | ATTTTATT others(36): Show |
1 | a0001c0001t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1051-331_1051-330i others(45): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616309 | A | T | 121 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1051-330T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | |||||||
| chr2:197616311 | A | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1051-332T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616311 | |||||||
| chr2:197616412 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG01243.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-433G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616412 | |||||||
| chr2:197616453 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051-474C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616453 | |||||||
| chr2:197616551 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1051-572A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616551 | |||||||
| chr2:197616653 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1051-674A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616653 | |||||||
| chr2:197616732 | G | A | 1 | a0001c0001t0026g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1051-753C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616732 | |||||||
| chr2:197616928 | C | A | 4 | a0001c0001t0003g0072 a0001c0001t0003g0175 a0001c0001t0003g0179 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050+872G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616928 | |||||||
| chr2:197617024 | G | A | 2 | a0001c0002t0002g0227 a0001c0002t0002g0229 |
2 | HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1050+776C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617024 | |||||||
| chr2:197617140 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1050+660T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617140 | |||||||
| chr2:197617247 | C | A | 1 | a0001c0001t0003g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1050+553G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617247 | |||||||
| chr2:197617258 | G | A | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+542C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617258 | |||||||
| chr2:197617364 | C | T | 1 | a0001c0001t0024g0085 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1050+436G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617364 | |||||||
| chr2:197617478 | A | G | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1050+322T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617478 | |||||||
| chr2:197617498 | C | T | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1050+302G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617498 | |||||||
| chr2:197618000 | CAT | C | 8 | a0001c0001t0003g0154 a0001c0001t0007g0078 a0001c0001t0011g0136 others(5): Show |
8 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-81_929-80delAT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618000 | |||||||
| chr2:197618061 | C | CCCCTCT | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(3): Show |
8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-146_929-141dup others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618061 | |||||||
| chr2:197618211 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.929-290C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618211 | |||||||
| chr2:197618246 | T | A | 1 | a0001c0002t0002g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.929-325A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618246 | |||||||
| chr2:197618319 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.929-398G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618319 | |||||||
| chr2:197618327 | A | G | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-406T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618327 | |||||||
| chr2:197618371 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-450C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618371 | |||||||
| chr2:197618454 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.929-533T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618454 | |||||||
| chr2:197618490 | C | T | 121 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-569G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618490 | |||||||
| chr2:197618493 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.929-572G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618493 | |||||||
| chr2:197618506 | A | AC | 8 | a0001c0001t0001g0304 a0001c0002t0002g0210 a0001c0002t0002g0221 others(5): Show |
8 | HG00621.hp1 HG00738.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-586dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618506 | |||||||
| chr2:197618568 | C | G | 3 | a0001c0001t0013g0048 a0001c0001t0013g0066 a0001c0001t0013g0101 |
3 | HG02818.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.929-647G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618568 | |||||||
| chr2:197618665 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.929-744T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618665 | |||||||
| chr2:197618690 | T | G | 1 | a0001c0001t0003g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.929-769A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618690 | |||||||
| chr2:197618734 | T | C | 2 | a0001c0002t0002g0256 a0001c0002t0031g0230 |
2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-813A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618734 | |||||||
| chr2:197618738 | G | A | 1 | a0001c0001t0007g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.929-817C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618738 | |||||||
| chr2:197618743 | G | A | 2 | a0001c0002t0002g0256 a0001c0002t0031g0230 |
2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-822C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618743 | |||||||
| chr2:197618746 | C | T | 2 | a0001c0002t0002g0256 a0001c0002t0031g0230 |
2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-825G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618746 | |||||||
| chr2:197618774 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-853G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618774 | |||||||
| chr2:197618791 | G | A | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.929-870C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618791 | |||||||
| chr2:197618859 | C | A | 2 | a0001c0001t0012g0041 a0001c0001t0012g0149 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.929-938G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618859 | |||||||
| chr2:197618875 | A | C | 2 | a0001c0001t0012g0041 a0001c0001t0012g0149 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.929-954T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618875 | |||||||
| chr2:197618879 | C | T | 15 | a0001c0001t0002g0119 a0001c0001t0005g0035 a0001c0001t0005g0074 others(12): Show |
15 | HG02027.hp1 HG02083.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-958G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618879 | |||||||
| chr2:197618943 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.929-1022G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618943 | |||||||
| chr2:197618955 | G | T | 20 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0002t0002g0183 others(17): Show |
20 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.929-1034C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618955 | |||||||
| chr2:197618975 | C | T | 1 | a0001c0002t0002g0277 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.929-1054G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618975 | |||||||
| chr2:197619106 | C | T | 9 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0062 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.929-1185G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619106 | |||||||
| chr2:197619115 | G | A | 1 | a0001c0002t0004g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.929-1194C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619115 | |||||||
| chr2:197619121 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-1200A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619121 | |||||||
| chr2:197619124 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-1203C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619124 | |||||||
| chr2:197619153 | A | G | 204 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.929-1232T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619153 | |||||||
| chr2:197619180 | C | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.929-1259G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619180 | |||||||
| chr2:197619243 | A | G | 71 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
73 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.929-1322T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619243 | |||||||
| chr2:197619248 | A | G | 71 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
73 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.929-1327T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619248 | |||||||
| chr2:197619250 | A | G | 71 | a0001c0001t0001g0192 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
73 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.929-1329T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619250 | |||||||
| chr2:197619291 | A | G | 11 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-1370T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619291 | |||||||
| chr2:197619334 | G | C | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-1413C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619334 | |||||||
| chr2:197619371 | G | C | 121 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-1450C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619371 | |||||||
| chr2:197619395 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.929-1474G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619395 | |||||||
| chr2:197619715 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.929-1794G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619715 | |||||||
| chr2:197619740 | T | TA | 82 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0043 others(79): Show |
82 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.929-1820dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619740 | |||||||
| chr2:197619740 | TA | T | 11 | a0001c0001t0011g0184 a0001c0002t0002g0216 a0001c0002t0002g0217 others(8): Show |
11 | HG02056.hp1 HG02486.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.929-1820delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619740 | |||||||
| chr2:197619750 | A | T | 1 | a0001c0001t0003g0025 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.929-1829T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619750 | |||||||
| chr2:197619751 | AAT | A | 8 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(5): Show |
8 | HG02886.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-1832_929-1831d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619751 | |||||||
| chr2:197619752 | AT | A | 14 | a0001c0001t0001g0137 a0001c0001t0001g0306 a0001c0001t0003g0044 others(11): Show |
14 | HG01081.hp2 HG01515.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-1832delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619752 | |||||||
| chr2:197619753 | T | A | 122 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.929-1832A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619753 | |||||||
| chr2:197619753 | T | TA | 5 | a0001c0001t0003g0062 a0001c0001t0009g0045 a0001c0001t0009g0046 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-1833dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619753 | |||||||
| chr2:197619756 | T | A | 15 | a0001c0001t0001g0071 a0001c0001t0001g0134 a0001c0001t0001g0161 others(12): Show |
15 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-1835A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619756 | |||||||
| chr2:197619759 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.929-1838A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619759 | |||||||
| chr2:197619762 | C | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.929-1841G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619762 | |||||||
| chr2:197619777 | A | G | 9 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(6): Show |
9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-1856T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619777 | |||||||
| chr2:197619865 | CT | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0003g0044 others(4): Show |
7 | HG01515.hp2 HG02015.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-1945delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619865 | |||||||
| chr2:197620174 | C | T | 1 | a0001c0001t0011g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.929-2253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620174 | |||||||
| chr2:197620458 | C | T | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.929-2537G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620458 | |||||||
| chr2:197620617 | A | C | 204 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.929-2696T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620617 | |||||||
| chr2:197620834 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.929-2913G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620834 | |||||||
| chr2:197620959 | C | G | 1 | a0001c0002t0007g0231 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.929-3038G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620959 | |||||||
| chr2:197620996 | A | C | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.929-3075T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620996 | |||||||
| chr2:197620997 | AAAAC | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0161 a0001c0001t0001g0180 others(5): Show |
8 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-3080_929-3077d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620997 | |||||||
| chr2:197621174 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.929-3253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621174 | |||||||
| chr2:197621257 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-3336A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621257 | |||||||
| chr2:197621401 | G | GT | 8 | a0001c0001t0001g0037 a0001c0001t0001g0134 a0001c0001t0003g0025 others(5): Show |
8 | HG00323.hp2 HG02965.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-3481dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | |||||||
| chr2:197621401 | G | GTT | 177 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.929-3482_929-3481d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | |||||||
| chr2:197621401 | G | GTTT | 15 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0068 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-3483_929-3481d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | |||||||
| chr2:197621510 | A | G | 2 | a0001c0001t0001g0114 a0001c0007t0001g0080 |
2 | HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.929-3589T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621510 | |||||||
| chr2:197621615 | C | T | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.929-3694G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621615 | |||||||
| chr2:197621881 | A | T | 1 | a0001c0001t0003g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.929-3960T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621881 | |||||||
| chr2:197622383 | C | T | 1 | a0001c0002t0003g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.929-4462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622383 | |||||||
| chr2:197622494 | C | T | 1 | a0001c0002t0030g0269 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.929-4573G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622494 | |||||||
| chr2:197622504 | C | T | 1 | a0001c0002t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.929-4583G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622504 | |||||||
| chr2:197622554 | C | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.929-4633G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622554 | |||||||
| chr2:197622604 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-4683G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622604 | |||||||
| chr2:197622647 | T | A | 2 | a0001c0001t0003g0165 a0001c0001t0006g0164 |
2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.929-4726A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622647 | |||||||
| chr2:197622721 | G | A | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-4800C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622721 | |||||||
| chr2:197622896 | C | G | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-4975G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622896 | |||||||
| chr2:197623048 | C | G | 1 | a0001c0001t0006g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.929-5127G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623048 | |||||||
| chr2:197623230 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.929-5309T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623230 | |||||||
| chr2:197623627 | C | T | 1 | a0001c0001t0006g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.929-5706G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623627 | |||||||
| chr2:197623698 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.929-5777G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623698 | |||||||
| chr2:197623744 | G | C | 121 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-5823C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623744 | |||||||
| chr2:197623915 | C | T | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.929-5994G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623915 | |||||||
| chr2:197623916 | G | A | 2 | a0001c0001t0019g0187 a0001c0002t0002g0264 |
2 | HG00738.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.929-5995C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623916 | |||||||
| chr2:197623961 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.929-6040C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623961 | |||||||
| chr2:197624050 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.929-6129G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624050 | |||||||
| chr2:197624172 | G | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.929-6251C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624172 | |||||||
| chr2:197624346 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-6425A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624346 | |||||||
| chr2:197624374 | C | T | 3 | a0001c0002t0004g0224 a0001c0002t0004g0225 a0001c0002t0004g0259 |
3 | NA18977.hp1 NA19075.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.929-6453G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624374 | |||||||
| chr2:197624375 | G | A | 1 | a0001c0002t0004g0291 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.929-6454C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624375 | |||||||
| chr2:197624389 | G | T | 2 | a0001c0001t0003g0154 a0001c0001t0011g0157 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.929-6468C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624389 | |||||||
| chr2:197624395 | G | C | 1 | a0001c0001t0007g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.929-6474C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624395 | |||||||
| chr2:197624484 | G | A | 1 | a0001c0001t0007g0092 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928+6527C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624484 | |||||||
| chr2:197624522 | C | T | 1 | a0001c0001t0005g0100 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.928+6489G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624522 | |||||||
| chr2:197624529 | C | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.928+6482G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624529 | |||||||
| chr2:197624585 | G | A | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+6426C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624585 | |||||||
| chr2:197624597 | C | CA | 18 | a0001c0001t0001g0084 a0001c0001t0004g0138 a0001c0001t0004g0139 others(15): Show |
18 | HG00673.hp2 HG01346.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.928+6413dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | |||||||
| chr2:197624597 | CA | C | 163 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.928+6413delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | |||||||
| chr2:197624597 | CAA | C | 12 | a0001c0001t0001g0037 a0001c0001t0003g0298 a0001c0001t0005g0035 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+6412_928+6413d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | |||||||
| chr2:197624597 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+6402_928+6413d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | |||||||
| chr2:197624616 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.928+6395T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624616 | |||||||
| chr2:197624636 | A | T | 1 | a0001c0001t0015g0120 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.928+6375T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624636 | |||||||
| chr2:197624687 | C | T | 9 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(6): Show |
9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+6324G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624687 | |||||||
| chr2:197624861 | A | G | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+6150T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624861 | |||||||
| chr2:197624883 | A | G | 121 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.928+6128T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624883 | |||||||
| chr2:197624888 | G | A | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+6123C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624888 | |||||||
| chr2:197625101 | T | G | 1 | a0001c0001t0003g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.928+5910A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625101 | |||||||
| chr2:197625473 | C | T | 2 | a0001c0001t0008g0057 a0001c0001t0010g0053 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.928+5538G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625473 | |||||||
| chr2:197625491 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5520T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625491 | |||||||
| chr2:197625663 | T | TCTCTC | 8 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0142 others(5): Show |
9 | HG01891.hp1 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+5343_928+5347d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | T | TCTCTCCT others(3): Show |
6 | a0001c0001t0003g0003 a0001c0001t0003g0143 a0001c0001t0008g0185 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+5338_928+5347d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | T | TCTCTCCT others(8): Show |
5 | a0001c0001t0003g0167 a0001c0001t0006g0152 a0001c0001t0008g0190 others(2): Show |
5 | HG02165.hp1 HG04199.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+5333_928+5347d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | T | TCTCTCCT others(13): Show |
2 | a0001c0001t0003g0168 a0001c0001t0008g0189 |
2 | HG00408.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.928+5328_928+5347d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | TCTCTC | T | 83 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0003g0013 others(80): Show |
83 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.928+5343_928+5347d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | TCTCTCCT others(3): Show |
T | 20 | a0001c0001t0003g0007 a0001c0001t0003g0038 a0001c0001t0003g0039 others(17): Show |
20 | HG00735.hp1 HG01106.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+5338_928+5347d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | TCTCTCCT others(8): Show |
T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0154 a0001c0001t0011g0136 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5333_928+5347d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625663 | TCTCTCCT others(13): Show |
T | 1 | a0001c0002t0002g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928+5328_928+5347d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | |||||||
| chr2:197625699 | C | CTCTCCTC others(23): Show |
4 | a0001c0001t0001g0073 a0001c0001t0007g0078 a0001c0001t0009g0135 others(1): Show |
4 | HG02809.hp1 HG02970.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(32): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | |||||||
| chr2:197625699 | C | CTCTCCTC others(18): Show |
6 | a0001c0001t0001g0113 a0001c0001t0002g0119 a0001c0001t0003g0062 others(3): Show |
6 | HG01884.hp1 HG02027.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(27): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | |||||||
| chr2:197625699 | C | CTCTCCTC others(13): Show |
82 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(79): Show |
82 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | |||||||
| chr2:197625699 | C | CTCTCCTC others(8): Show |
21 | a0001c0001t0001g0042 a0001c0001t0001g0089 a0001c0001t0001g0122 others(18): Show |
21 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | |||||||
| chr2:197625699 | C | CTCTCCTC others(3): Show |
8 | a0001c0001t0001g0180 a0001c0001t0001g0205 a0001c0001t0001g0207 others(5): Show |
8 | HG01168.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | |||||||
| chr2:197625729 | T | C | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928+5282A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625729 | |||||||
| chr2:197625731 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.928+5280G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625731 | |||||||
| chr2:197625983 | T | G | 1 | a0001c0001t0003g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.928+5028A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625983 | |||||||
| chr2:197625989 | G | A | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 |
3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+5022C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625989 | |||||||
| chr2:197626014 | C | G | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928+4997G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626014 | |||||||
| chr2:197626026 | T | G | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+4985A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626026 | |||||||
| chr2:197626078 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+4933G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626078 | |||||||
| chr2:197626376 | G | A | 3 | a0001c0002t0002g0005 a0001c0002t0002g0198 a0001c0002t0002g0222 |
3 | HG00558.hp2 HG02165.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.928+4635C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626376 | |||||||
| chr2:197626386 | C | T | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.928+4625G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626386 | |||||||
| chr2:197626456 | C | T | 116 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.928+4555G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626456 | |||||||
| chr2:197626526 | T | G | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928+4485A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626526 | |||||||
| chr2:197626562 | C | CAAAT | 5 | a0001c0001t0003g0154 a0001c0001t0011g0136 a0001c0001t0011g0157 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+4445_928+4448d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | C | CAAATAAA others(1): Show |
173 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.928+4441_928+4448d others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | C | CAAATAAA others(5): Show |
18 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(15): Show |
20 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+4437_928+4448d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | C | CAAATAAA others(9): Show |
4 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0147 others(1): Show |
4 | HG02015.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+4433_928+4448d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | C | CAAATAAA others(13): Show |
2 | a0001c0001t0006g0150 a0001c0001t0006g0151 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+4429_928+4448d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | C | CAAATAAA others(17): Show |
1 | a0001c0001t0006g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928+4425_928+4448d others(26): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626562 | CAAAT | C | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+4445_928+4448d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | |||||||
| chr2:197626614 | C | CT | 75 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(72): Show |
75 | HG00408.hp2 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.928+4396dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | |||||||
| chr2:197626614 | C | CTT | 19 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0090 others(16): Show |
19 | HG00621.hp2 HG01243.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.928+4395_928+4396d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | |||||||
| chr2:197626614 | C | CTTT | 7 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0205 others(4): Show |
7 | HG01891.hp2 HG02148.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+4396_928+4397i others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | |||||||
| chr2:197626617 | C | CT | 9 | a0001c0001t0003g0003 a0001c0001t0003g0064 a0001c0001t0003g0142 others(6): Show |
11 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.928+4393dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | |||||||
| chr2:197626617 | C | CTT | 63 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(60): Show |
65 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.928+4392_928+4393d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | |||||||
| chr2:197626617 | C | CTTT | 15 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0013 others(12): Show |
15 | HG01361.hp1 HG02055.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+4391_928+4393d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | |||||||
| chr2:197626617 | C | T | 120 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.928+4394G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | |||||||
| chr2:197626617 | CT | C | 81 | a0001c0001t0002g0155 a0001c0002t0002g0005 a0001c0002t0002g0133 others(78): Show |
81 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.928+4393delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | |||||||
| chr2:197626756 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0007g0067 |
2 | HG00621.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.928+4255G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626756 | |||||||
| chr2:197626767 | C | G | 1 | a0001c0002t0002g0297 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928+4244G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626767 | |||||||
| chr2:197626784 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+4227G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626784 | |||||||
| chr2:197627105 | G | A | 1 | a0001c0001t0010g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928+3906C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627105 | |||||||
| chr2:197627191 | C | T | 1 | a0001c0002t0002g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.928+3820G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627191 | |||||||
| chr2:197627592 | T | G | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.928+3419A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627592 | |||||||
| chr2:197627622 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0011g0188 a0001c0001t0022g0031 |
3 | HG02280.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.928+3389A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627622 | |||||||
| chr2:197627647 | G | C | 2 | a0001c0001t0008g0189 a0001c0001t0008g0190 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928+3364C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627647 | |||||||
| chr2:197627694 | G | A | 1 | a0001c0001t0007g0092 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928+3317C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627694 | |||||||
| chr2:197627874 | C | T | 65 | a0001c0001t0001g0073 a0001c0001t0001g0147 a0001c0001t0001g0161 others(62): Show |
67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+3137G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627874 | |||||||
| chr2:197627875 | G | C | 1 | a0001c0001t0005g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.928+3136C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627875 | |||||||
| chr2:197627883 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0126 |
2 | NA18961.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.928+3128C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | |||||||
| chr2:197627883 | G | C | 1 | a0001c0002t0004g0225 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.928+3128C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | |||||||
| chr2:197627883 | G | GC | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0003g0019 others(9): Show |
12 | HG01192.hp1 HG01934.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+3127dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | |||||||
| chr2:197627885 | C | G | 1 | a0001c0001t0006g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928+3126G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627885 | |||||||
| chr2:197627911 | T | C | 1 | a0001c0002t0002g0251 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.928+3100A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627911 | |||||||
| chr2:197628102 | C | T | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+2909G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628102 | |||||||
| chr2:197628103 | C | T | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+2908G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628103 | |||||||
| chr2:197628113 | C | T | 124 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.928+2898G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628113 | |||||||
| chr2:197628180 | C | CT | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+2830dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628180 | |||||||
| chr2:197628219 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+2792A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628219 | |||||||
| chr2:197628313 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0025 |
2 | HG00323.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.928+2698C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628313 | |||||||
| chr2:197628343 | G | A | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+2668C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628343 | |||||||
| chr2:197628362 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928+2649G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628362 | |||||||
| chr2:197628616 | GA | G | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+2394delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628616 | |||||||
| chr2:197628758 | G | A | 1 | a0001c0002t0002g0297 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928+2253C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628758 | |||||||
| chr2:197628880 | C | T | 3 | a0001c0002t0002g0270 a0001c0002t0004g0290 a0001c0002t0030g0269 |
3 | HG01993.hp1 HG02004.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.928+2131G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628880 | |||||||
| chr2:197628979 | T | A | 115 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(112): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.928+2032A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628979 | |||||||
| chr2:197629002 | G | A | 1 | a0001c0001t0026g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928+2009C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629002 | |||||||
| chr2:197629094 | C | G | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+1917G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629094 | |||||||
| chr2:197629165 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.928+1846T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629165 | |||||||
| chr2:197629245 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0022g0031 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.928+1766G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629245 | |||||||
| chr2:197629282 | C | A | 64 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(61): Show |
66 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.928+1729G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629282 | |||||||
| chr2:197629341 | A | C | 99 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.928+1670T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629341 | |||||||
| chr2:197629387 | C | T | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.928+1624G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629387 | |||||||
| chr2:197629466 | G | T | 1 | a0001c0002t0002g0229 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928+1545C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629466 | |||||||
| chr2:197629560 | A | G | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+1451T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629560 | |||||||
| chr2:197629622 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.928+1389C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629622 | |||||||
| chr2:197629675 | T | TAC | 14 | a0001c0001t0001g0106 a0001c0001t0001g0137 a0001c0001t0003g0051 others(11): Show |
14 | HG01258.hp2 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.928+1334_928+1335d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACAC | 14 | a0001c0001t0001g0172 a0001c0001t0003g0038 a0001c0001t0003g0039 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.928+1332_928+1335d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACAC | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(6): Show |
9 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+1330_928+1335d others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(3): Show |
12 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0003g0044 others(9): Show |
12 | HG01069.hp1 HG01106.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.928+1326_928+1335d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(5): Show |
3 | a0001c0001t0003g0170 a0001c0001t0006g0152 a0005c0005t0006g0153 |
3 | HG01070.hp2 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.928+1324_928+1335d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(7): Show |
23 | a0001c0001t0001g0192 a0001c0001t0002g0155 a0001c0001t0002g0156 others(20): Show |
24 | HG00323.hp2 HG00408.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.928+1322_928+1335d others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(9): Show |
5 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0026 others(2): Show |
5 | HG02083.hp1 HG02145.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+1320_928+1335d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(11): Show |
6 | a0001c0001t0003g0002 a0001c0001t0003g0021 a0001c0001t0003g0022 others(3): Show |
7 | HG02886.hp2 NA18939.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.928+1318_928+1335d others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(13): Show |
3 | a0001c0001t0003g0014 a0001c0001t0012g0041 a0001c0001t0012g0149 |
3 | HG02717.hp2 HG03139.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.928+1316_928+1335d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | T | TACACACA others(15): Show |
2 | a0001c0001t0006g0150 a0001c0001t0006g0151 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+1314_928+1335d others(24): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629675 | TAC | T | 6 | a0001c0001t0001g0296 a0001c0001t0003g0003 a0001c0001t0003g0142 others(3): Show |
8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+1334_928+1335d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | |||||||
| chr2:197629696 | A | ACACACAC others(13): Show |
1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.928+1314_928+1315i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629696 | |||||||
| chr2:197629696 | A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928+1314_928+1315i others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629696 | |||||||
| chr2:197629697 | C | T | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1314G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629697 | |||||||
| chr2:197629699 | C | T | 3 | a0001c0002t0002g0243 a0001c0002t0002g0244 a0001c0002t0002g0265 |
3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1312G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629699 | |||||||
| chr2:197629700 | A | T | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1311T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629700 | |||||||
| chr2:197629701 | T | C | 101 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.928+1310A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629701 | |||||||
| chr2:197629702 | A | ACACATAT others(4): Show |
2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.928+1308_928+1309i others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629702 | A | ATATTTAT | 98 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.928+1308_928+1309i others(9): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629702 | A | ATTTAT | 84 | a0001c0002t0001g0197 a0001c0002t0002g0005 a0001c0002t0002g0133 others(81): Show |
84 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.928+1304_928+1308d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629702 | A | ATTTATTT others(3): Show |
15 | a0001c0002t0002g0221 a0001c0002t0002g0245 a0001c0002t0002g0246 others(12): Show |
15 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+1299_928+1308d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629702 | A | ATTTATTT others(8): Show |
3 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0285 |
3 | NA18946.hp2 NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.928+1294_928+1308d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629702 | A | T | 1 | a0001c0002t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.928+1309T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | |||||||
| chr2:197629731 | A | T | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+1280T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629731 | |||||||
| chr2:197629736 | T | A | 9 | a0001c0002t0002g0221 a0001c0002t0002g0245 a0001c0002t0002g0246 others(6): Show |
9 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.928+1275A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629736 | |||||||
| chr2:197629744 | A | G | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.928+1267T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629744 | |||||||
| chr2:197629777 | T | C | 1 | a0001c0006t0006g0169 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.928+1234A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629777 | |||||||
| chr2:197629809 | A | T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0065 a0001c0001t0013g0066 |
3 | HG02818.hp2 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.928+1202T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629809 | |||||||
| chr2:197629935 | G | C | 6 | a0001c0001t0001g0296 a0001c0001t0003g0003 a0001c0001t0003g0142 others(3): Show |
8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+1076C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629935 | |||||||
| chr2:197630004 | G | A | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+1007C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630004 | |||||||
| chr2:197630058 | C | T | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.928+953G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630058 | |||||||
| chr2:197630078 | C | T | 1 | a0001c0002t0002g0293 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.928+933G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630078 | |||||||
| chr2:197630103 | T | C | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+908A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630103 | |||||||
| chr2:197630208 | TAATA | T | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.928+799_928+802del others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630208 | |||||||
| chr2:197630388 | T | C | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928+623A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630388 | |||||||
| chr2:197630535 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.928+476T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630535 | |||||||
| chr2:197630553 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.928+458G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630553 | |||||||
| chr2:197630696 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+315G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630696 | |||||||
| chr2:197630707 | G | C | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.928+304C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630707 | |||||||
| chr2:197630858 | A | G | 1 | a0001c0002t0002g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.928+153T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630858 | |||||||
| chr2:197631255 | A | G | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-35T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631255 | |||||||
| chr2:197631322 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.719-102C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631322 | |||||||
| chr2:197631566 | G | C | 1 | a0001c0002t0002g0254 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.719-346C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631566 | |||||||
| chr2:197631605 | T | C | 4 | a0001c0002t0002g0248 a0001c0002t0002g0250 a0001c0002t0002g0251 others(1): Show |
4 | NA18944.hp1 NA18950.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-385A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631605 | |||||||
| chr2:197631614 | A | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.719-394T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631614 | |||||||
| chr2:197631959 | A | AC | 6 | a0001c0001t0005g0097 a0001c0001t0007g0092 a0001c0002t0002g0005 others(3): Show |
6 | HG01099.hp1 HG01175.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.719-740dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631959 | |||||||
| chr2:197632003 | A | G | 1 | a0001c0001t0003g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.719-783T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632003 | |||||||
| chr2:197632027 | A | C | 1 | a0001c0002t0002g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.719-807T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632027 | |||||||
| chr2:197632064 | A | G | 3 | a0001c0002t0002g0266 a0001c0002t0002g0267 a0001c0002t0002g0293 |
3 | HG01928.hp2 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.719-844T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632064 | |||||||
| chr2:197632381 | C | T | 52 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(49): Show |
54 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.719-1161G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632381 | |||||||
| chr2:197632452 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0022g0031 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.719-1232A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632452 | |||||||
| chr2:197632525 | T | C | 1 | a0001c0001t0003g0023 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.718+1193A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632525 | |||||||
| chr2:197632631 | C | T | 1 | a0001c0001t0007g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.718+1087G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632631 | |||||||
| chr2:197632699 | G | A | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+1019C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632699 | |||||||
| chr2:197632788 | T | G | 137 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.718+930A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632788 | |||||||
| chr2:197632985 | C | T | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.718+733G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632985 | |||||||
| chr2:197633008 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718+710C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633008 | |||||||
| chr2:197633011 | T | A | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718+707A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633011 | |||||||
| chr2:197633022 | A | T | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.718+696T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633022 | |||||||
| chr2:197633319 | T | G | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+399A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633319 | |||||||
| chr2:197633328 | A | T | 2 | a0002c0003t0002g0226 a0002c0003t0002g0255 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.718+390T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633328 | |||||||
| chr2:197633536 | A | G | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.718+182T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633536 | |||||||
| chr2:197633592 | T | G | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.718+126A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633592 | |||||||
| chr2:197634050 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.439-53A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634050 | |||||||
| chr2:197634061 | A | G | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.439-64T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634061 | |||||||
| chr2:197634333 | A | G | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.439-336T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634333 | |||||||
| chr2:197634438 | C | T | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-441G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634438 | |||||||
| chr2:197634692 | ATTTTTTA others(4): Show |
A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-706_439-696del others(11): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634692 | |||||||
| chr2:197634699 | AT | A | 9 | a0001c0001t0001g0128 a0001c0001t0003g0003 a0001c0001t0003g0051 others(6): Show |
11 | HG00408.hp2 HG01261.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-703delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634699 | |||||||
| chr2:197634703 | T | A | 1 | a0001c0002t0002g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.439-706A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634703 | |||||||
| chr2:197634720 | ATTAT | A | 55 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(52): Show |
57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.439-727_439-724del others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634720 | |||||||
| chr2:197634720 | ATTATTTA others(1): Show |
A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-731_439-724del others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634720 | |||||||
| chr2:197634814 | A | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-817T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634814 | |||||||
| chr2:197634832 | C | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-835G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634832 | |||||||
| chr2:197634850 | A | G | 1 | a0001c0002t0002g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.439-853T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634850 | |||||||
| chr2:197634874 | T | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-877A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634874 | |||||||
| chr2:197634977 | A | T | 1 | a0001c0002t0002g0277 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.439-980T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634977 | |||||||
| chr2:197634983 | G | A | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-986C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634983 | |||||||
| chr2:197634991 | G | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-994C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634991 | |||||||
| chr2:197634991 | G | GT | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.439-995dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634991 | |||||||
| chr2:197635005 | C | T | 57 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(54): Show |
59 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.439-1008G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635005 | |||||||
| chr2:197635128 | G | T | 191 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.439-1131C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635128 | |||||||
| chr2:197635167 | T | A | 15 | a0001c0001t0002g0119 a0001c0001t0005g0035 a0001c0001t0005g0074 others(12): Show |
15 | HG02027.hp1 HG02083.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.439-1170A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635167 | |||||||
| chr2:197635199 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-1202A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635199 | |||||||
| chr2:197635231 | T | C | 137 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.439-1234A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635231 | |||||||
| chr2:197635294 | T | A | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1297A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635294 | |||||||
| chr2:197635295 | C | A | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1298G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635295 | |||||||
| chr2:197635296 | C | A | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1299G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635296 | |||||||
| chr2:197635297 | C | G | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1300G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635297 | |||||||
| chr2:197635299 | G | C | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1302C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635299 | |||||||
| chr2:197635304 | G | C | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1307C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635304 | |||||||
| chr2:197635326 | C | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-1329G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635326 | |||||||
| chr2:197635342 | C | T | 1 | a0001c0002t0002g0289 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439-1345G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635342 | |||||||
| chr2:197635423 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1426T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635423 | |||||||
| chr2:197635428 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-1431A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635428 | |||||||
| chr2:197635511 | A | G | 1 | a0001c0001t0009g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439-1514T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635511 | |||||||
| chr2:197635514 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.439-1517A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635514 | |||||||
| chr2:197635546 | T | G | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-1549A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635546 | |||||||
| chr2:197635553 | T | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1556A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635553 | |||||||
| chr2:197635637 | G | C | 1 | a0001c0001t0003g0026 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.439-1640C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635637 | |||||||
| chr2:197635734 | T | G | 1 | a0001c0002t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.439-1737A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635734 | |||||||
| chr2:197635951 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.439-1954G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635951 | |||||||
| chr2:197635972 | C | G | 1 | a0001c0001t0003g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.439-1975G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635972 | |||||||
| chr2:197636030 | C | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-2033G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636030 | |||||||
| chr2:197636055 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-2058G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636055 | |||||||
| chr2:197636083 | T | C | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-2086A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636083 | |||||||
| chr2:197636192 | T | C | 1 | a0005c0005t0006g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.439-2195A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636192 | |||||||
| chr2:197636242 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-2245C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636242 | |||||||
| chr2:197636293 | T | G | 133 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.439-2296A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636293 | |||||||
| chr2:197636453 | A | C | 3 | a0001c0002t0004g0224 a0001c0002t0004g0225 a0001c0002t0004g0259 |
3 | NA18977.hp1 NA19075.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.439-2456T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636453 | |||||||
| chr2:197636485 | T | A | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-2488A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636485 | |||||||
| chr2:197636743 | C | A | 2 | a0001c0002t0002g0266 a0001c0002t0002g0267 |
2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.439-2746G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636743 | |||||||
| chr2:197636763 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-2766G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636763 | |||||||
| chr2:197636835 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-2838G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636835 | |||||||
| chr2:197637053 | T | C | 1 | a0001c0002t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.439-3056A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637053 | |||||||
| chr2:197637062 | A | T | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.439-3065T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637062 | |||||||
| chr2:197637096 | G | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-3099C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637096 | |||||||
| chr2:197637135 | G | A | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-3138C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637135 | |||||||
| chr2:197637247 | A | G | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-3250T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637247 | |||||||
| chr2:197637271 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0022g0031 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.439-3274C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637271 | |||||||
| chr2:197637376 | C | G | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-3379G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637376 | |||||||
| chr2:197637529 | G | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-3532C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637529 | |||||||
| chr2:197637551 | A | T | 2 | a0001c0002t0003g0199 a0001c0002t0034g0200 |
2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.439-3554T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637551 | |||||||
| chr2:197637652 | G | T | 137 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.439-3655C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637652 | |||||||
| chr2:197637838 | C | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-3841G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637838 | |||||||
| chr2:197637914 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-3917T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637914 | |||||||
| chr2:197637951 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.439-3954A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637951 | |||||||
| chr2:197637989 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.439-3992C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637989 | |||||||
| chr2:197637997 | T | C | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.439-4000A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637997 | |||||||
| chr2:197638031 | C | T | 1 | a0001c0001t0027g0109 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.439-4034G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638031 | |||||||
| chr2:197638045 | G | A | 1 | a0001c0002t0002g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.439-4048C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638045 | |||||||
| chr2:197638046 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.439-4049C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638046 | |||||||
| chr2:197638057 | A | G | 304 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.439-4060T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638057 | |||||||
| chr2:197638072 | G | T | 1 | a0001c0001t0007g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439-4075C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638072 | |||||||
| chr2:197638118 | T | C | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-4121A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638118 | |||||||
| chr2:197638159 | C | G | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-4162G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638159 | |||||||
| chr2:197638165 | G | C | 1 | a0001c0001t0009g0046 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.439-4168C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638165 | |||||||
| chr2:197638226 | G | C | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-4229C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638226 | |||||||
| chr2:197638253 | A | G | 80 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(77): Show |
80 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.439-4256T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638253 | |||||||
| chr2:197638256 | C | T | 83 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(80): Show |
83 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.439-4259G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638256 | |||||||
| chr2:197638295 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-4298C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638295 | |||||||
| chr2:197638311 | G | A | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.439-4314C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638311 | |||||||
| chr2:197638326 | G | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-4329C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638326 | |||||||
| chr2:197638439 | T | A | 1 | a0001c0001t0006g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.439-4442A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638439 | |||||||
| chr2:197638460 | T | C | 1 | a0001c0001t0006g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.439-4463A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638460 | |||||||
| chr2:197638563 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0017g0299 |
2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.439-4566G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638563 | |||||||
| chr2:197638564 | T | C | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.439-4567A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638564 | |||||||
| chr2:197638568 | C | T | 1 | a0001c0002t0002g0297 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.439-4571G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638568 | |||||||
| chr2:197638576 | GT | G | 4 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(1): Show |
6 | HG02559.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-4580delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638576 | |||||||
| chr2:197638627 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-4630C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638627 | |||||||
| chr2:197638784 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.439-4787C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638784 | |||||||
| chr2:197638797 | T | G | 1 | a0001c0002t0004g0259 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.439-4800A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638797 | |||||||
| chr2:197638836 | G | A | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-4839C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638836 | |||||||
| chr2:197638868 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-4871G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638868 | |||||||
| chr2:197638878 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.439-4881G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638878 | |||||||
| chr2:197638881 | T | G | 1 | a0001c0002t0002g0203 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.439-4884A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638881 | |||||||
| chr2:197638882 | T | G | 1 | a0001c0002t0002g0203 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.439-4885A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638882 | |||||||
| chr2:197638950 | G | C | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.439-4953C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638950 | |||||||
| chr2:197638969 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.439-4972A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638969 | |||||||
| chr2:197639099 | C | T | 2 | a0001c0001t0003g0064 a0001c0001t0003g0173 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438+5059G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639099 | |||||||
| chr2:197639102 | G | C | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0286 |
3 | NA18950.hp2 NA18963.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.438+5056C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639102 | |||||||
| chr2:197639145 | T | C | 2 | a0001c0002t0002g0193 a0001c0002t0002g0194 |
2 | HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.438+5013A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639145 | |||||||
| chr2:197639235 | G | A | 1 | a0001c0002t0004g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.438+4923C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639235 | |||||||
| chr2:197639253 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+4905C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639253 | |||||||
| chr2:197639260 | G | C | 1 | a0003c0004t0001g0125 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.438+4898C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639260 | |||||||
| chr2:197639354 | C | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+4804G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639354 | |||||||
| chr2:197639358 | G | C | 1 | a0001c0001t0003g0016 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.438+4800C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639358 | |||||||
| chr2:197639559 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.438+4599G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639559 | |||||||
| chr2:197639559 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.438+4599G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639559 | |||||||
| chr2:197639648 | T | A | 1 | a0001c0001t0003g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.438+4510A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639648 | |||||||
| chr2:197639715 | C | T | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.438+4443G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639715 | |||||||
| chr2:197639741 | G | C | 1 | a0001c0001t0002g0155 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.438+4417C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639741 | |||||||
| chr2:197639754 | T | C | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+4404A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639754 | |||||||
| chr2:197639771 | T | C | 4 | a0001c0001t0019g0187 a0001c0002t0002g0217 a0001c0002t0002g0219 others(1): Show |
4 | HG03225.hp1 NA18948.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+4387A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639771 | |||||||
| chr2:197639791 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+4367C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639791 | |||||||
| chr2:197639811 | G | A | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+4347C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639811 | |||||||
| chr2:197639812 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.438+4346G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639812 | |||||||
| chr2:197639813 | G | A | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.438+4345C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639813 | |||||||
| chr2:197639820 | G | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+4338C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639820 | |||||||
| chr2:197639834 | A | C | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.438+4324T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639834 | |||||||
| chr2:197639973 | A | C | 1 | a0001c0002t0002g0218 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.438+4185T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639973 | |||||||
| chr2:197639999 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+4159C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639999 | |||||||
| chr2:197640006 | A | G | 1 | a0001c0002t0003g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4152T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640006 | |||||||
| chr2:197640051 | A | G | 2 | a0001c0001t0003g0016 a0001c0002t0003g0260 |
2 | NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.438+4107T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640051 | |||||||
| chr2:197640084 | G | C | 2 | a0001c0001t0003g0063 a0001c0002t0003g0260 |
2 | HG02886.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.438+4074C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640084 | |||||||
| chr2:197640093 | C | G | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.438+4065G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640093 | |||||||
| chr2:197640094 | G | A | 1 | a0001c0002t0003g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4064C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640094 | |||||||
| chr2:197640123 | G | A | 1 | a0001c0002t0003g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4035C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640123 | |||||||
| chr2:197640178 | A | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3980T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640178 | |||||||
| chr2:197640219 | C | G | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.438+3939G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640219 | |||||||
| chr2:197640269 | G | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3889C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640269 | |||||||
| chr2:197640278 | T | C | 6 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG00323.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+3880A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640278 | |||||||
| chr2:197640279 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3879C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640279 | |||||||
| chr2:197640299 | G | C | 7 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+3859C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640299 | |||||||
| chr2:197640330 | C | T | 1 | a0001c0001t0014g0015 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.438+3828G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640330 | |||||||
| chr2:197640420 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3738G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640420 | |||||||
| chr2:197640421 | C | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3737G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640421 | |||||||
| chr2:197640441 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3717C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640441 | |||||||
| chr2:197640465 | A | T | 1 | a0001c0002t0002g0254 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.438+3693T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640465 | |||||||
| chr2:197640484 | A | T | 52 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(49): Show |
54 | HG00323.hp2 HG00408.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.438+3674T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640484 | |||||||
| chr2:197640489 | C | G | 127 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.438+3669G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640489 | |||||||
| chr2:197640537 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.438+3621C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640537 | |||||||
| chr2:197640542 | C | T | 137 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.438+3616G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640542 | |||||||
| chr2:197640543 | C | T | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.438+3615G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640543 | |||||||
| chr2:197640580 | G | A | 1 | a0001c0002t0002g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.438+3578C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640580 | |||||||
| chr2:197640639 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.438+3519G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640639 | |||||||
| chr2:197640658 | C | T | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.438+3500G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640658 | |||||||
| chr2:197640687 | CCCGTCTT others(3): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438+3461_438+3470d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640687 | |||||||
| chr2:197640725 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3433C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640725 | |||||||
| chr2:197640744 | C | T | 80 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(77): Show |
80 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.438+3414G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640744 | |||||||
| chr2:197640869 | TTTA | T | 3 | a0001c0001t0001g0161 a0001c0001t0003g0044 a0001c0001t0003g0160 |
3 | HG01069.hp1 HG01515.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.438+3286_438+3288d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640869 | |||||||
| chr2:197640881 | C | G | 1 | a0001c0002t0002g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.438+3277G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640881 | |||||||
| chr2:197640940 | A | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+3218T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640940 | |||||||
| chr2:197641278 | T | C | 5 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.438+2880A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641278 | |||||||
| chr2:197641742 | C | T | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.438+2416G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641742 | |||||||
| chr2:197641758 | C | T | 13 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.438+2400G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641758 | |||||||
| chr2:197641807 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.438+2351C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641807 | |||||||
| chr2:197641924 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.438+2234G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641924 | |||||||
| chr2:197641962 | C | T | 7 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0008g0057 others(4): Show |
7 | HG02922.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.438+2196G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641962 | |||||||
| chr2:197641966 | A | G | 304 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.438+2192T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641966 | |||||||
| chr2:197642416 | T | C | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+1742A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642416 | |||||||
| chr2:197642535 | A | G | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+1623T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642535 | |||||||
| chr2:197642794 | G | T | 1 | a0001c0001t0006g0004 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.438+1364C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642794 | |||||||
| chr2:197642923 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.438+1235C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642923 | |||||||
| chr2:197642925 | G | A | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.438+1233C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642925 | |||||||
| chr2:197642998 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | NA18939.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.438+1160A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642998 | |||||||
| chr2:197642998 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.438+1160A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642998 | |||||||
| chr2:197643010 | C | T | 1 | a0001c0002t0004g0223 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.438+1148G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643010 | |||||||
| chr2:197643067 | T | G | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0029g0052 |
3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.438+1091A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643067 | |||||||
| chr2:197643289 | G | C | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.438+869C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643289 | |||||||
| chr2:197643292 | A | G | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.438+866T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643292 | |||||||
| chr2:197643320 | T | C | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.438+838A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643320 | |||||||
| chr2:197643320 | T | TGGCCTCA others(11): Show |
1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.438+820_438+837dup others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643320 | |||||||
| chr2:197643400 | G | C | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+758C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643400 | |||||||
| chr2:197644148 | A | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+10T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197644148 | |||||||
| chr2:197644334 | C | T | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.324-62G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644334 | |||||||
| chr2:197644476 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324-204C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644476 | |||||||
| chr2:197644726 | G | C | 2 | a0001c0002t0003g0199 a0001c0002t0034g0200 |
2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.324-454C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644726 | |||||||
| chr2:197645041 | G | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.324-769C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645041 | |||||||
| chr2:197645387 | C | A | 1 | a0001c0002t0033g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.323+1096G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645387 | |||||||
| chr2:197645460 | AG | A | 16 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(13): Show |
16 | HG00099.hp2 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.323+1022delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645460 | |||||||
| chr2:197645516 | A | G | 1 | a0001c0001t0009g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323+967T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645516 | |||||||
| chr2:197645567 | A | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0065 a0001c0001t0013g0066 |
3 | HG02818.hp2 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+916T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645567 | |||||||
| chr2:197645940 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+543G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645940 | |||||||
| chr2:197646267 | C | T | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.323+216G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646267 | |||||||
| chr2:197646362 | G | A | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.323+121C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646362 | |||||||
| chr2:197646380 | C | T | 1 | a0005c0005t0006g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.323+103G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646380 | |||||||
| chr2:197646420 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.323+63A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646420 | |||||||
| chr2:197646433 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.323+50G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646433 | |||||||
| chr2:197646450 | C | T | 1 | a0001c0001t0011g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+33G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646450 | |||||||
| chr2:197646886 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.140-220G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646886 | |||||||
| chr2:197646897 | C | CA | 198 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.140-232dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646897 | |||||||
| chr2:197646897 | C | CAA | 43 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0107 others(40): Show |
44 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.140-233_140-232dup others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646897 | |||||||
| chr2:197646908 | A | AAC | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-243_140-242ins others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646908 | |||||||
| chr2:197646911 | A | C | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.140-245T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646911 | |||||||
| chr2:197647116 | A | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-450T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647116 | |||||||
| chr2:197647193 | A | G | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.140-527T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647193 | |||||||
| chr2:197647249 | G | T | 4 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(1): Show |
4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-583C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647249 | |||||||
| chr2:197647368 | C | G | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.140-702G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647368 | |||||||
| chr2:197647800 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.140-1134T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647800 | |||||||
| chr2:197647876 | AAG | A | 3 | a0001c0002t0001g0263 a0001c0002t0002g0261 a0001c0002t0002g0262 |
3 | HG01261.hp2 HG02698.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.140-1212_140-1211d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647876 | |||||||
| chr2:197648050 | C | T | 5 | a0001c0001t0008g0057 a0001c0001t0010g0053 a0001c0001t0010g0054 others(2): Show |
5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.140-1384G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648050 | |||||||
| chr2:197648125 | G | A | 138 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.140-1459C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648125 | |||||||
| chr2:197648281 | A | C | 1 | a0001c0002t0002g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.140-1615T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648281 | |||||||
| chr2:197648285 | A | C | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-1619T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648285 | |||||||
| chr2:197649153 | C | T | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.140-2487G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649153 | |||||||
| chr2:197649206 | G | A | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.140-2540C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649206 | |||||||
| chr2:197649283 | T | C | 1 | a0001c0001t0016g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140-2617A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649283 | |||||||
| chr2:197649750 | A | G | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-3084T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649750 | |||||||
| chr2:197649847 | A | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-3181T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649847 | |||||||
| chr2:197649914 | A | C | 11 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-3248T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649914 | |||||||
| chr2:197649953 | T | C | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-3287A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649953 | |||||||
| chr2:197649964 | A | G | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-3298T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649964 | |||||||
| chr2:197650121 | G | A | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-3455C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650121 | |||||||
| chr2:197650151 | G | T | 1 | a0001c0002t0002g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.140-3485C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650151 | |||||||
| chr2:197650200 | C | T | 131 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.140-3534G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650200 | |||||||
| chr2:197650526 | C | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-3860G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650526 | |||||||
| chr2:197650530 | G | A | 4 | a0001c0002t0002g0213 a0001c0002t0002g0218 a0001c0002t0002g0264 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-3864C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650530 | |||||||
| chr2:197650727 | A | G | 4 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(1): Show |
4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-4061T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650727 | |||||||
| chr2:197650755 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.140-4089C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650755 | |||||||
| chr2:197650812 | G | A | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.140-4146C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650812 | |||||||
| chr2:197650934 | T | C | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.140-4268A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650934 | |||||||
| chr2:197651134 | G | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.140-4468C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651134 | |||||||
| chr2:197651176 | G | A | 197 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.140-4510C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651176 | |||||||
| chr2:197651285 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.140-4619A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651285 | |||||||
| chr2:197651345 | G | A | 2 | a0001c0002t0002g0272 a0001c0002t0032g0273 |
2 | HG00639.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.140-4679C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651345 | |||||||
| chr2:197651356 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140-4690G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651356 | |||||||
| chr2:197651361 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-4695C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651361 | |||||||
| chr2:197651544 | G | A | 1 | a0001c0001t0005g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.140-4878C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651544 | |||||||
| chr2:197651571 | G | A | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-4905C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651571 | |||||||
| chr2:197651587 | G | A | 1 | a0001c0001t0009g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.140-4921C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651587 | |||||||
| chr2:197651592 | G | A | 2 | a0001c0001t0005g0123 a0001c0002t0002g0277 |
2 | NA19068.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.140-4926C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651592 | |||||||
| chr2:197651626 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-4960T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651626 | |||||||
| chr2:197651639 | C | A | 2 | a0001c0002t0002g0275 a0001c0002t0002g0276 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.140-4973G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651639 | |||||||
| chr2:197652077 | C | G | 1 | a0001c0002t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.140-5411G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652077 | |||||||
| chr2:197652097 | C | T | 102 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.140-5431G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652097 | |||||||
| chr2:197652111 | G | A | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.140-5445C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652111 | |||||||
| chr2:197652868 | A | G | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-6202T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652868 | |||||||
| chr2:197652916 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140-6250T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652916 | |||||||
| chr2:197653169 | C | T | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-6503G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653169 | |||||||
| chr2:197653182 | T | G | 1 | a0001c0001t0005g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.140-6516A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653182 | |||||||
| chr2:197653318 | T | C | 1 | a0001c0001t0003g0029 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.140-6652A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653318 | |||||||
| chr2:197653338 | C | T | 55 | a0001c0001t0001g0077 a0001c0001t0001g0108 a0001c0001t0001g0147 others(52): Show |
57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.140-6672G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653338 | |||||||
| chr2:197653612 | G | A | 1 | a0001c0002t0004g0282 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.140-6946C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653612 | |||||||
| chr2:197653716 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.140-7050G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653716 | |||||||
| chr2:197653777 | T | C | 1 | a0001c0002t0028g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.140-7111A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653777 | |||||||
| chr2:197653985 | C | G | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-7319G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653985 | |||||||
| chr2:197654061 | G | A | 1 | a0005c0005t0006g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.140-7395C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654061 | |||||||
| chr2:197654162 | C | T | 4 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0006g0151 others(1): Show |
4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-7496G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654162 | |||||||
| chr2:197654227 | A | T | 1 | a0001c0001t0003g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.140-7561T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654227 | |||||||
| chr2:197654590 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.140-7924C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654590 | |||||||
| chr2:197654764 | G | A | 6 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-8098C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654764 | |||||||
| chr2:197654864 | G | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-8198C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654864 | |||||||
| chr2:197654904 | T | C | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.140-8238A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654904 | |||||||
| chr2:197655179 | A | G | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-8513T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655179 | |||||||
| chr2:197655591 | C | T | 1 | a0001c0002t0002g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-8925G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655591 | |||||||
| chr2:197655658 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140-8992A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655658 | |||||||
| chr2:197655770 | G | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-9104C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655770 | |||||||
| chr2:197655817 | C | T | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0029g0052 |
3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-9151G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655817 | |||||||
| chr2:197655831 | A | C | 52 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(49): Show |
54 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.140-9165T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655831 | |||||||
| chr2:197655891 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.140-9225T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655891 | |||||||
| chr2:197655929 | A | T | 3 | a0001c0002t0002g0217 a0001c0002t0002g0219 a0001c0002t0002g0220 |
3 | NA18948.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.140-9263T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655929 | |||||||
| chr2:197655964 | C | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-9298G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655964 | |||||||
| chr2:197656068 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.140-9402C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656068 | |||||||
| chr2:197656266 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140-9600C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656266 | |||||||
| chr2:197656632 | T | C | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.140-9966A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656632 | |||||||
| chr2:197656683 | C | G | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-10017G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656683 | |||||||
| chr2:197656766 | C | T | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-10100G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656766 | |||||||
| chr2:197656782 | G | A | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.140-10116C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656782 | |||||||
| chr2:197656833 | A | G | 1 | a0001c0002t0002g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.140-10167T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656833 | |||||||
| chr2:197656914 | C | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-10248G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656914 | |||||||
| chr2:197657025 | TA | T | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.140-10360delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657025 | |||||||
| chr2:197657026 | A | T | 48 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(45): Show |
50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-10360T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657026 | |||||||
| chr2:197657036 | A | T | 2 | a0001c0001t0001g0126 a0001c0001t0003g0158 |
2 | HG01361.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.140-10370T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657036 | |||||||
| chr2:197657402 | T | C | 94 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(91): Show |
94 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.140-10736A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657402 | |||||||
| chr2:197657668 | TG | T | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-11003delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657668 | |||||||
| chr2:197657783 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0093 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.140-11117C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657783 | |||||||
| chr2:197657908 | A | G | 190 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(187): Show |
194 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.140-11242T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657908 | |||||||
| chr2:197657911 | C | G | 139 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.140-11245G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657911 | |||||||
| chr2:197658045 | T | C | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-11379A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658045 | |||||||
| chr2:197658073 | G | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0075 others(7): Show |
10 | HG00735.hp2 HG01258.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.140-11407C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658073 | |||||||
| chr2:197658179 | AT | A | 193 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-11514delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658179 | |||||||
| chr2:197658182 | T | A | 2 | a0001c0001t0017g0299 a0001c0001t0018g0307 |
2 | HG02015.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.140-11516A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658182 | |||||||
| chr2:197658220 | G | A | 2 | a0001c0001t0013g0048 a0001c0001t0013g0101 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.140-11554C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658220 | |||||||
| chr2:197658284 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.140-11618T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658284 | |||||||
| chr2:197658292 | G | T | 1 | a0001c0001t0007g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140-11626C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658292 | |||||||
| chr2:197658300 | A | G | 1 | a0001c0001t0005g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.140-11634T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658300 | |||||||
| chr2:197658331 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.140-11665G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658331 | |||||||
| chr2:197658347 | C | T | 1 | a0001c0001t0019g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-11681G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658347 | |||||||
| chr2:197658449 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0022g0031 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140-11783T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658449 | |||||||
| chr2:197658452 | GT | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0298 a0001c0001t0008g0057 others(11): Show |
14 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.140-11787delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658452 | |||||||
| chr2:197658452 | GTT | G | 178 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(175): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.140-11788_140-1178 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658452 | |||||||
| chr2:197658455 | T | G | 1 | a0003c0004t0001g0125 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.140-11789A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658455 | |||||||
| chr2:197658477 | G | C | 2 | a0001c0001t0001g0071 a0001c0001t0003g0094 |
2 | HG00642.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.140-11811C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658477 | |||||||
| chr2:197658615 | A | G | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-11949T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658615 | |||||||
| chr2:197658656 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-11990T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658656 | |||||||
| chr2:197658678 | T | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.140-12012A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658678 | |||||||
| chr2:197658817 | T | C | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-12151A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658817 | |||||||
| chr2:197659016 | G | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-12350C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659016 | |||||||
| chr2:197659225 | G | A | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-12559C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659225 | |||||||
| chr2:197659301 | C | A | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-12635G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659301 | |||||||
| chr2:197659381 | C | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-12715G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659381 | |||||||
| chr2:197659425 | C | T | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-12759G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659425 | |||||||
| chr2:197659477 | TA | T | 125 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.140-12812delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659477 | |||||||
| chr2:197659477 | TAA | T | 68 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0002g0155 others(65): Show |
70 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.140-12813_140-1281 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659477 | |||||||
| chr2:197659478 | A | T | 1 | a0001c0001t0011g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.140-12812T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659478 | |||||||
| chr2:197659554 | A | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-12888T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659554 | |||||||
| chr2:197659557 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-12891G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659557 | |||||||
| chr2:197659584 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12918C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659584 | |||||||
| chr2:197659586 | G | C | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12920C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659586 | |||||||
| chr2:197659587 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12921C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659587 | |||||||
| chr2:197659589 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12923C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659589 | |||||||
| chr2:197659590 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12924C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659590 | |||||||
| chr2:197659804 | CA | C | 195 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.140-13139delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659804 | |||||||
| chr2:197659847 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140-13181T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659847 | |||||||
| chr2:197660161 | G | C | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.140-13495C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660161 | |||||||
| chr2:197660297 | TTA | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-13633_140-1363 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660297 | |||||||
| chr2:197660313 | A | C | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-13647T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660313 | |||||||
| chr2:197660360 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.140-13694T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660360 | |||||||
| chr2:197660384 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-13718G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660384 | |||||||
| chr2:197660397 | A | G | 1 | a0001c0002t0004g0274 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.140-13731T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660397 | |||||||
| chr2:197660445 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.140-13779C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660445 | |||||||
| chr2:197660587 | C | CT | 6 | a0001c0001t0001g0177 a0001c0001t0004g0138 a0001c0001t0004g0139 others(3): Show |
6 | HG02615.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-13922dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660587 | |||||||
| chr2:197660651 | G | T | 1 | a0001c0001t0029g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-13985C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660651 | |||||||
| chr2:197660755 | C | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0001t0012g0149 |
3 | HG02886.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.140-14089G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660755 | |||||||
| chr2:197660854 | C | T | 1 | a0001c0001t0003g0012 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.140-14188G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660854 | |||||||
| chr2:197661233 | AT | A | 191 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.139+14086delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661233 | |||||||
| chr2:197661273 | G | C | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+14047C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661273 | |||||||
| chr2:197661364 | G | A | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+13956C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661364 | |||||||
| chr2:197661811 | G | C | 2 | a0001c0002t0002g0266 a0001c0002t0002g0267 |
2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.139+13509C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661811 | |||||||
| chr2:197662114 | C | T | 1 | a0001c0001t0011g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+13206G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662114 | |||||||
| chr2:197662507 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.139+12813G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662507 | |||||||
| chr2:197662616 | A | T | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139+12704T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662616 | |||||||
| chr2:197662616 | AT | A | 8 | a0001c0002t0002g0183 a0001c0002t0002g0268 a0001c0002t0002g0270 others(5): Show |
8 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+12703delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662616 | |||||||
| chr2:197662647 | C | T | 200 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.139+12673G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662647 | |||||||
| chr2:197662743 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+12577A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662743 | |||||||
| chr2:197662783 | A | T | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+12537T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662783 | |||||||
| chr2:197662827 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.139+12493G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662827 | |||||||
| chr2:197662966 | A | G | 1 | a0001c0001t0008g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.139+12354T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662966 | |||||||
| chr2:197663270 | T | C | 2 | a0001c0002t0004g0283 a0001c0002t0004g0284 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.139+12050A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663270 | |||||||
| chr2:197663418 | G | A | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0029g0052 |
3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139+11902C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663418 | |||||||
| chr2:197663443 | T | C | 1 | a0001c0001t0025g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.139+11877A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663443 | |||||||
| chr2:197663606 | G | T | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+11714C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663606 | |||||||
| chr2:197663624 | A | C | 1 | a0001c0001t0003g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.139+11696T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663624 | |||||||
| chr2:197663691 | G | A | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0029g0052 |
3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139+11629C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663691 | |||||||
| chr2:197663783 | T | A | 4 | a0001c0001t0003g0072 a0001c0001t0003g0175 a0001c0001t0003g0179 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+11537A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663783 | |||||||
| chr2:197663984 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.139+11336A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663984 | |||||||
| chr2:197664157 | C | T | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+11163G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664157 | |||||||
| chr2:197664275 | C | T | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+11045G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664275 | |||||||
| chr2:197664302 | G | A | 8 | a0001c0002t0002g0183 a0001c0002t0002g0268 a0001c0002t0002g0270 others(5): Show |
8 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+11018C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664302 | |||||||
| chr2:197664446 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139+10874C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664446 | |||||||
| chr2:197664475 | CA | C | 164 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.139+10844delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664475 | |||||||
| chr2:197664475 | CAA | C | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0003g0001 others(25): Show |
30 | HG00323.hp2 HG01192.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.139+10843_139+1084 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664475 | |||||||
| chr2:197664502 | C | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10818G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664502 | |||||||
| chr2:197664513 | G | T | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+10807C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664513 | |||||||
| chr2:197664586 | A | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+10734T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664586 | |||||||
| chr2:197664740 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10580C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664740 | |||||||
| chr2:197664772 | G | A | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.139+10548C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664772 | |||||||
| chr2:197664825 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.139+10495T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664825 | |||||||
| chr2:197664930 | C | T | 7 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+10390G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664930 | |||||||
| chr2:197664931 | G | A | 1 | a0001c0002t0004g0274 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.139+10389C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664931 | |||||||
| chr2:197665212 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+10108C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665212 | |||||||
| chr2:197665224 | C | A | 5 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0005g0097 others(2): Show |
5 | HG00558.hp1 NA18986.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10096G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665224 | |||||||
| chr2:197665233 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10087G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665233 | |||||||
| chr2:197665234 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10086A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665234 | |||||||
| chr2:197665235 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10085A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665235 | |||||||
| chr2:197665237 | C | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10083G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665237 | |||||||
| chr2:197665239 | G | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10081C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665239 | |||||||
| chr2:197665241 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10079A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665241 | |||||||
| chr2:197665242 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10078G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665242 | |||||||
| chr2:197665243 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10077T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665243 | |||||||
| chr2:197665248 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10072A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665248 | |||||||
| chr2:197665250 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10070T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665250 | |||||||
| chr2:197665252 | G | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10068C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665252 | |||||||
| chr2:197665255 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10065T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665255 | |||||||
| chr2:197665256 | A | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10064T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665256 | |||||||
| chr2:197665258 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10062G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665258 | |||||||
| chr2:197665261 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10059T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665261 | |||||||
| chr2:197665264 | C | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10056G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665264 | |||||||
| chr2:197665267 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10053G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665267 | |||||||
| chr2:197665269 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10051G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665269 | |||||||
| chr2:197665270 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10050T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665270 | |||||||
| chr2:197665272 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10048T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665272 | |||||||
| chr2:197665276 | A | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10044T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665276 | |||||||
| chr2:197665278 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10042T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665278 | |||||||
| chr2:197665281 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10039G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665281 | |||||||
| chr2:197665283 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10037T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665283 | |||||||
| chr2:197665284 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10036A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665284 | |||||||
| chr2:197665289 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10031A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665289 | |||||||
| chr2:197665293 | A | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10027T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665293 | |||||||
| chr2:197665294 | A | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10026T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665294 | |||||||
| chr2:197665296 | A | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10024T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665296 | |||||||
| chr2:197665299 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10021A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665299 | |||||||
| chr2:197665311 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10009A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665311 | |||||||
| chr2:197665313 | C | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10007G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665313 | |||||||
| chr2:197665315 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10005A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665315 | |||||||
| chr2:197665316 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10004A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665316 | |||||||
| chr2:197665319 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10001A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665319 | |||||||
| chr2:197665320 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10000T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665320 | |||||||
| chr2:197665321 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9999A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665321 | |||||||
| chr2:197665322 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9998A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665322 | |||||||
| chr2:197665323 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9997A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665323 | |||||||
| chr2:197665325 | C | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9995G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665325 | |||||||
| chr2:197665326 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9994A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665326 | |||||||
| chr2:197665329 | C | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9991G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665329 | |||||||
| chr2:197665330 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9990A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665330 | |||||||
| chr2:197665331 | G | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9989C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665331 | |||||||
| chr2:197665373 | T | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9947A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665373 | |||||||
| chr2:197665378 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9942A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665378 | |||||||
| chr2:197665439 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9881A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665439 | |||||||
| chr2:197665440 | C | G | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9880G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665440 | |||||||
| chr2:197665443 | G | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9877C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665443 | |||||||
| chr2:197665508 | G | A | 5 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0005g0097 others(2): Show |
5 | HG00558.hp1 NA18986.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+9812C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665508 | |||||||
| chr2:197665517 | C | CTTTTTTT others(3): Show |
36 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(33): Show |
38 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.139+9793_139+9802d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0147 a0001c0001t0003g0006 a0001c0001t0003g0012 others(8): Show |
11 | HG01243.hp1 HG01516.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+9792_139+9802d others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0022g0031 a0001c0001t0029g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.139+9791_139+9802d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0018g0307 |
3 | HG02015.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.139+9790_139+9802d others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(7): Show |
4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0006g0148 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+9789_139+9802d others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0306 a0001c0001t0005g0181 |
2 | HG01081.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.139+9787_139+9802d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(10): Show |
56 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0042 others(53): Show |
57 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(19): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(11): Show |
53 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0043 others(50): Show |
54 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(12): Show |
14 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(11): Show |
14 | HG00642.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(21): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0068 others(5): Show |
8 | HG00621.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665517 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0134 a0001c0001t0003g0065 |
2 | HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.139+9802_139+9803i others(23): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | |||||||
| chr2:197665542 | C | T | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+9778G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665542 | |||||||
| chr2:197665569 | G | A | 139 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.139+9751C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665569 | |||||||
| chr2:197665631 | C | T | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+9689G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665631 | |||||||
| chr2:197665634 | C | G | 1 | a0001c0001t0003g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139+9686G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665634 | |||||||
| chr2:197665776 | A | ACTGATAT others(2): Show |
53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.139+9535_139+9543d others(11): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665776 | |||||||
| chr2:197665907 | C | G | 1 | a0001c0002t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.139+9413G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665907 | |||||||
| chr2:197666205 | C | A | 3 | a0001c0002t0002g0202 a0001c0002t0002g0203 a0004c0008t0002g0204 |
3 | HG01255.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.139+9115G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666205 | |||||||
| chr2:197666334 | C | A | 2 | a0001c0002t0002g0275 a0001c0002t0002g0276 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.139+8986G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666334 | |||||||
| chr2:197666360 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+8960T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666360 | |||||||
| chr2:197666507 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.139+8813A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666507 | |||||||
| chr2:197666543 | A | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+8777T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666543 | |||||||
| chr2:197666660 | C | T | 1 | a0001c0002t0002g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+8660G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666660 | |||||||
| chr2:197666700 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.139+8620A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666700 | |||||||
| chr2:197666805 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+8515T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666805 | |||||||
| chr2:197667041 | T | C | 11 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+8279A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667041 | |||||||
| chr2:197667059 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+8261C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667059 | |||||||
| chr2:197667564 | T | C | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+7756A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667564 | |||||||
| chr2:197668053 | A | G | 6 | a0001c0001t0001g0296 a0001c0001t0003g0003 a0001c0001t0003g0142 others(3): Show |
8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+7267T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668053 | |||||||
| chr2:197668270 | A | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+7050T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668270 | |||||||
| chr2:197668302 | C | T | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+7018G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668302 | |||||||
| chr2:197668340 | C | T | 1 | a0001c0001t0009g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.139+6980G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668340 | |||||||
| chr2:197668385 | C | T | 1 | a0001c0001t0005g0174 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.139+6935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668385 | |||||||
| chr2:197668458 | A | G | 11 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+6862T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668458 | |||||||
| chr2:197668527 | C | T | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.139+6793G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668527 | |||||||
| chr2:197668563 | C | T | 2 | a0001c0002t0002g0211 a0001c0002t0002g0212 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.139+6757G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668563 | |||||||
| chr2:197668645 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+6675T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668645 | |||||||
| chr2:197668882 | G | T | 139 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.139+6438C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668882 | |||||||
| chr2:197668950 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+6370T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668950 | |||||||
| chr2:197669376 | C | CT | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+5943dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669376 | |||||||
| chr2:197669477 | C | G | 2 | a0001c0001t0016g0140 a0001c0001t0016g0141 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.139+5843G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669477 | |||||||
| chr2:197669552 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.139+5768G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669552 | |||||||
| chr2:197669591 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.139+5729T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669591 | |||||||
| chr2:197669636 | C | T | 12 | a0001c0001t0008g0057 a0001c0001t0008g0185 a0001c0001t0008g0186 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.139+5684G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669636 | |||||||
| chr2:197669775 | T | A | 1 | a0001c0002t0002g0277 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.139+5545A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669775 | |||||||
| chr2:197669790 | C | T | 192 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+5530G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669790 | |||||||
| chr2:197669967 | C | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+5353G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669967 | |||||||
| chr2:197669984 | G | A | 126 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+5336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669984 | |||||||
| chr2:197670252 | T | G | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+5068A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670252 | |||||||
| chr2:197670273 | A | G | 3 | a0001c0002t0002g0202 a0001c0002t0002g0203 a0004c0008t0002g0204 |
3 | HG01255.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.139+5047T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670273 | |||||||
| chr2:197670384 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0007g0171 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139+4936G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670384 | |||||||
| chr2:197670483 | C | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+4837G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670483 | |||||||
| chr2:197670580 | CAGG | C | 47 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0002g0155 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.139+4737_139+4739d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670580 | |||||||
| chr2:197670732 | TA | T | 58 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(55): Show |
60 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.139+4587delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670732 | |||||||
| chr2:197670830 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.139+4490G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670830 | |||||||
| chr2:197670871 | G | A | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+4449C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670871 | |||||||
| chr2:197670954 | T | C | 179 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0147 others(176): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.139+4366A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670954 | |||||||
| chr2:197670955 | G | A | 54 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(51): Show |
56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+4365C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670955 | |||||||
| chr2:197671006 | A | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.139+4314T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671006 | |||||||
| chr2:197671154 | A | T | 2 | a0001c0002t0003g0199 a0001c0002t0034g0200 |
2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.139+4166T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671154 | |||||||
| chr2:197671423 | C | T | 4 | a0001c0001t0009g0045 a0001c0001t0009g0046 a0001c0001t0009g0047 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+3897G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671423 | |||||||
| chr2:197671448 | C | T | 1 | a0001c0002t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.139+3872G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671448 | |||||||
| chr2:197671615 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+3705A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671615 | |||||||
| chr2:197671658 | A | G | 6 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(3): Show |
6 | HG00673.hp1 HG02015.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.139+3662T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671658 | |||||||
| chr2:197671661 | A | T | 1 | a0001c0002t0002g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.139+3659T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671661 | |||||||
| chr2:197671730 | G | T | 1 | a0001c0001t0022g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139+3590C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671730 | |||||||
| chr2:197671855 | CT | C | 4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0016g0140 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3464delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671855 | |||||||
| chr2:197672175 | T | A | 5 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+3145A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672175 | |||||||
| chr2:197672336 | T | C | 5 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0143 others(2): Show |
7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+2984A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672336 | |||||||
| chr2:197672557 | A | G | 53 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0192 others(50): Show |
55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.139+2763T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672557 | |||||||
| chr2:197672641 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.139+2679T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672641 | |||||||
| chr2:197672679 | T | C | 1 | a0001c0001t0005g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.139+2641A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672679 | |||||||
| chr2:197672923 | T | G | 5 | a0001c0002t0004g0280 a0001c0002t0004g0282 a0001c0002t0004g0283 others(2): Show |
5 | HG02055.hp2 HG03491.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+2397A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672923 | |||||||
| chr2:197673049 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.139+2271G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673049 | |||||||
| chr2:197673132 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.139+2188G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673132 | |||||||
| chr2:197673228 | C | A | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+2092G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673228 | |||||||
| chr2:197673716 | G | A | 1 | a0001c0001t0011g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.139+1604C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673716 | |||||||
| chr2:197673807 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0017g0299 |
2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.139+1513G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673807 | |||||||
| chr2:197673967 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.139+1353T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673967 | |||||||
| chr2:197674063 | C | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+1257G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674063 | |||||||
| chr2:197674073 | G | A | 2 | a0001c0001t0008g0189 a0001c0001t0008g0190 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.139+1247C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674073 | |||||||
| chr2:197674116 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.139+1204T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674116 | |||||||
| chr2:197674339 | C | CA | 69 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0172 others(66): Show |
71 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.139+980dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | |||||||
| chr2:197674339 | C | CAA | 95 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0001g0205 others(92): Show |
95 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.139+979_139+980dup others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | |||||||
| chr2:197674339 | C | CAAA | 12 | a0001c0002t0001g0285 a0001c0002t0002g0286 a0001c0002t0002g0289 others(9): Show |
12 | HG01928.hp1 HG01978.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.139+978_139+980dup others(3): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | |||||||
| chr2:197674339 | CA | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG02015.hp2 HG02970.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+980delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | |||||||
| chr2:197674359 | A | G | 1 | a0001c0001t0020g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+961T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674359 | |||||||
| chr2:197674620 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139+700A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674620 | |||||||
| chr2:197674681 | A | G | 24 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(21): Show |
26 | HG00323.hp2 HG01192.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.139+639T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674681 | |||||||
| chr2:197674739 | T | C | 1 | a0001c0002t0002g0297 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.139+581A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674739 | |||||||
| chr2:197674776 | C | T | 2 | a0001c0002t0012g0008 a0001c0002t0028g0009 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.139+544G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674776 | |||||||
| chr2:197674791 | CT | C | 8 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
8 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+528delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674791 | |||||||
| chr2:197674821 | A | G | 1 | a0001c0001t0003g0007 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.139+499T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674821 | |||||||
| chr2:197674921 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.139+399G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674921 | |||||||
| chr2:197675130 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.139+190A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675130 | |||||||
| chr2:197675172 | A | G | 1 | a0001c0002t0002g0005 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.139+148T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675172 | |||||||
| chr2:197675242 | T | G | 1 | a0001c0001t0018g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+78A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675242 | |||||||
| chr2:197675295 | C | T | 5 | a0001c0001t0008g0185 a0001c0001t0008g0186 a0001c0001t0008g0189 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+25G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675295 |